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UK CRA Jobs

UK CRA Jobs

Search and apply for jobs now or set up a  job alert  to hear about new roles as soon as they are posted.

Popular CRA Jobs:

  • Clinical Research Associate (CRA)
  • Senior Clinical Research Associate (SCRA)
  • Freelance CRA
  • Outsourced CRA
  • Home based CRA
  • Start up CRA

More Clinical Research Jobs in the UK:

  • Clinical Trials Manager / Administrator
  • Clinical Operations
  • Clinical Development
  • Clinical Project Manager
  • Study Start Up
  • Pharmacovigilance
  • Clinical Study Manager
  • Drug Safety
  • Clinical Program Manager

All UK Clinical Research Jobs

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Found 13 jobs in this campaign

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CRA II - North West

Fortrea logo

  • Maidenhead, United Kingdom
  • Competitive

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortre...

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  • 12 days ago
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Senior Clinical Research Associate - UK - FSP

Parexel logo

  • United Kingdom

Parexel is currently seeking Senior Clinical Research Associates. Home-based in the UK. Working as a Senior Clinical Research Associate at Parexel...

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Sponsor Dedicated Sr CRA II - UK wide (Must have Rare disease exp

Syneos Health logo

  • United Kingdom; Homeworking
  • Syneos Health

FSP Senior Clinical Research Associate II Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...

View details Sponsor Dedicated Sr CRA II - UK wide (Must have Rare disease exp

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Clinical Research Associate, UK

ICON Strategic Solutions logo

  • United Kingdom, Homeworking
  • ICON Strategic Solutions

Experienced UK-based Regional CRA/clinical research associate required to augment existing CRA team, for multinational biopharmaceutical company partn

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Clinical Research Associate II

Additional Job Description Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical service...

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  • 20 days ago
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Clinical Research Associate - Biopharma

Experienced England, UK-based CRA/clinical research associate required to augment existing non-Oncology CRA team, for pharmaceutical and biotechnology

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Clinical Research Associate - M4 corridor

Role: Clinical Research Associate Location: South West England/South Midlands (must be within a commuteable distance to Oxford, Bristol, Birmingha

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Clinical Research Associate II - UK - FSP

Parexel is currently seeking Clinical Research Associate IIs. Home-based in the UK. Working as a Clinical Research Associate II at Parexel FSP offe...

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Clinical Research Associate - must be based in the North of England

Role: Clinical Research Associate Locatio n: North England - ideally Central based so you can cover both the East and West, but we would consider N

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Senior CRA / CRA II

ICON Plc logo

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research provid

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  • Ireland, United Kingdom, Homeworking

About the role ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical

  • 11 days ago

As a Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This

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Clinical research associate

Clinical drug research is a competitive but growing field and work experience in a scientific or healthcare environment is crucial for a job as a clinical research associate

As a clinical research associate (CRA), you'll run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use.

You'll work on new and existing drugs and will typically be involved in all stages of the clinical trial, including identifying an investigational site and setting up, initiating, monitoring and closing down the trial.

Clinical trials may be carried out at various stages or phases and include trials on healthy humans, trials on patients with a disease, and studies conducted after the launch of a new drug to monitor safety and side effects.

Responsibilities

Tasks vary depending on your employer and level of experience. However, you'll typically need to:

  • develop and write trial protocols (outlining purpose and methodology)
  • present trial protocols to a steering committee
  • design data collection forms, known as case report forms (CRFs)
  • coordinate with the ethics committee, which safeguards the rights, safety and wellbeing of all trial subjects
  • manage regulatory authority applications and approvals that oversee the research and marketing of new and existing drugs
  • identify and assess the suitability of facilities to use as the clinical trial site
  • identify/select an investigator who will be responsible for conducting the trial at the trial site
  • liaise with doctors, consultants or investigators on conducting the trial
  • set up the trial sites - ensuring each centre has the trial materials, including the trial drug often known as the investigational medicinal product (IMP)
  • train the site staff to trial-specific industry standards
  • monitor the trial throughout its duration, which involves visiting the trial sites on a regular basis and dealing with and solving any issues
  • verify that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)
  • collect completed CRFs from hospitals and general practices
  • write visit reports and file and collate trial documentation and reports
  • meet with team members to discuss on-going trials, results and any trends or adverse events
  • ensure all unused trial supplies are accounted for
  • close down trial sites on completion of the trial
  • discuss results with a medical statistician, who writes technical trial reports
  • archive study documentation and correspondence
  • prepare final reports and occasionally manuscripts for publication.
  • Starting salaries for CRAs are in the region of £26,000 to £34,000. It's likely these posts will require some experience in a related area.
  • As a senior CRA (SCRA), also known as a CRA II, you can earn a salary of around £35,000 to £50,000.
  • In some senior roles, as a manager or director, salaries of in excess of £55,000 can be achieved.

Salaries vary from company to company. Additional benefits, such as a car allowance and bonus and pension, are typically offered.

Income figures are intended as a guide only.

Working hours

Working conditions vary between companies, although the hours are usually full time, Monday to Friday. You should expect to work some evenings, although weekend or shift work is uncommon.

Part-time work is possible, as are career breaks. Short term contracts of six to 12 months with a company are common, meaning you may work more like a contractor than a permanent employee.

What to expect

  • It's likely your role will be a mixture of desk-based work and site visits. You'll visit trial sites to set up and close down a trial as well as to monitor the trial while it is running which could involve visits every four to six weeks. Some trials may be running abroad which will involve international travel. There may be opportunities for home-working the remainder of the time. In some instances you may find a role that is almost exclusively office-based with the focus being on document review.
  • Most UK pharmaceutical companies are located in the south of England. Field-based positions are generally found in key locations throughout the UK. Some jobs, for example in a company laboratory, can be found locally, while others are regionally based.
  • Self-employment or freelance work is possible once you've gained significant experience.
  • The job can involve a lot of travelling and you may be out of the office three or four days a week, possibly including overnight stays. Some companies operate a system whereby the CRA specialises in a specific disease area and covers the whole of the UK. Others operate their CRAs on a regional basis.
  • Initiatives are in place to encourage more women into science-based careers, such as Women in STEM .

Qualifications

To become a clinical research associate (CRA) you need to have a degree in life sciences, medical sciences or nursing.

This could include subjects such as:

  • biochemistry
  • biomedical science
  • microbiology
  • molecular biology
  • pharmacology or pharmacy
  • toxicology.

Entry without a degree or with a HND only is unlikely. You might occasionally be able to enter from the administration side - for example, you could start as a study-site coordinator in the NHS or as a clinical trials administrator/assistant. However, you would need substantial experience and further qualifications to progress to the role of CRA.

A postgraduate qualification is not essential, with many employers only looking for a related undergraduate degree. However, it could give you valuable experience in clinical trials and may be an advantage against competition when applying for jobs. A relevant PhD can also be advantageous in some companies, who may consider it as highly-relevant work experience counting towards gaining promotion to senior positions or moving into protocol development. Check with desired employers to find out what they're looking for.

Search for postgraduate courses in clinical research or clinical trials .

You'll need to have:

  • excellent communication, both written and verbal, and interpersonal skills
  • the ability to build effective relationships with trial centre staff and colleagues
  • the ability to motivate others
  • strong customer focus
  • an excellent grasp of numeracy and a keen eye for detail
  • presentation skills
  • the ability to multitask and think on your feet
  • project management skills
  • a flexible and adaptable approach to work
  • organisational, IT and administrative skills - the job involves a lot of documenting and recording information through computerised processes, such as clinical trial management systems and electronic data capture
  • an understanding of the importance of good clinical practice (GCP) , which is a legal requirement for all CRAs.

You'll usually need a clean driving licence for travel between trial sites and your office.

Skills in an additional language, particularly any European ones, may also be useful for roles abroad.

Work experience

Relevant experience is crucial for securing a job as a CRA. Without it, you're likely to start work at a lower level, as a clinical data coordinator or clinical trials administrator/assistant, where you won't be involved in initiating or designing the trials. Once you've gained experience, you will then move on to a full CRA position.

A small number of companies may recruit graduates without experience if they have the necessary personal skills, but it's more likely that employers will look for someone who has some actual experience in a related workplace. This can include any work that uses scientific and analytical skills, for example:

  • academic or pharmaceutical research
  • clinical data work
  • clinical laboratory work
  • medical sales
  • nursing or care work

Another useful way of gaining experience is to complete an industrial placement as part of your undergraduate degree. This can give you the real-world experience in a related area as well as helping you to make contacts that could lead to potential job offers in the future.

Competition for jobs is strong and work experience in a clinically-relevant field will considerably improve your chances.

For free mentoring resources and experiences designed to support aspiring healthcare and legal professionals - including virtual work experience that is accepted by medical schools, see Medic Mentor .

Find out more about the different kinds of  work experience and internships  that are available.

Typical employers include pharmaceutical companies, medical device manufacturers, biotech companies and contract research organisations (CROs), which conduct research on behalf of pharmaceutical companies.

A CRO will organise the placement of a CRA on behalf of the sponsor (the pharmaceutical company) and may be involved in planning, organising and conducting the whole study or just part of it. The CRA will report back to the organisation and will feed back to the sponsor.

Large contract organisations are more likely to recruit an inexperienced graduate into a monitoring role and provide the training to progress to the level of a CRA.

Hospital academic departments occasionally employ CRAs in clinical trials units.

Look for job vacancies at:

  • BMJ Careers
  • emedcareers
  • New Scientist Jobs
  • Pharmiweb Jobs

Contract research organisations and pharmaceutical companies may advertise vacancies on their own websites.

Specialist recruitment agencies also handle vacancies. These include AL Solutions and RBW Consulting .

Professional development

Training takes place mainly in-house and on the job. The nature of the training can vary from company to company, with some employers providing a structured system.

Some companies will pay for relevant external training courses through organisations such as the Institute of Clinical Research (ICR) . They provide training in areas such as:

  • advanced monitoring
  • effective project management for clinical trials
  • essentials of clinical trial monitoring
  • process thinking in clinical trials.

You can also complete the ICR Certificate and Diploma to provide evidence of your clinical research knowledge and skills.

Becoming a member of the ICR can aid career development as it provides networking opportunities, discounted training, specialist interest groups and access to industry news. You can progress through the ICR membership levels but to do so you'll need to undertake a certain amount of continuing professional development (CPD) each year.

If you don't already have a postgraduate qualification, you can take a postgraduate certificate, diploma or Masters in areas such as:

  • clinical pharmacology
  • clinical pharmacy
  • clinical research
  • pharmaceutical medicine.

It's also possible to do a PhD. These courses can facilitate professional development and career advancement but you should check this against the career route you want to follow and employers of interest.

Career prospects

Career structures vary from company to company. How quickly you move up the grades depends on a range of factors including motivation, the opportunities available for training and development, ability and previous experience.

Before becoming a CRA, you may begin at a lower level such as a clinical trial administrator or junior CRA. As a CRA (also known as a CRA I), you'll work on pre-trial procedures, setting up and organising clinical trial sites (with some supervision), archiving documents and correspondence.

With the right combination of skills and experience you can move into the role of senior CRA (SCRA), also known as a CRA II. Work will include selecting investigators, coordinating ethics committee and regulatory authority applications, supervising trial supplies and attending investigator meetings.

As you progress further you'll also be responsible for supervising, training and mentoring junior staff, project management of whole trials (possibly on an international scale), protocol development and design of case report forms (CRFs). You could become a clinical team manager, clinical trial manager or clinical project manager depending on where your interests and skills lie. Beyond this are director roles within the same areas.

If you work within a contract research organisation you can build up and widen your experience with a variety of sponsor pharmaceutical companies in different therapeutic areas and in different phases of clinical research. This could allow you to move to a pharmaceutical company.

Self-employment may be possible as CRAs are employed on a freelance basis by certain companies. This should usually only be considered when you have developed experience, contacts and clients.

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Job Opportunities

Clinical research associate (fixed term).

Mr Adel Helmy is looking for a Clinical Research Fellow to join his research group based on the Cambridge Biomedical Campus.

This role will support an MRC funded research grant exploring the cellular constituents of the brain following acute brain injury (subarachnoid haemorrhage and traumatic brain injury), with a focus on neuroinflammation. It is an ideal role for a neurosurgical trainee with an interest in research, ideally working towards a higher degree.

In the first instance, funding is available for 1 year of full time salary. There are additional opportunities within the clinical department for on-call contribution to the neurosurgical clinical service.

You will require GMC registration, License to Practice and Medical Defence Cover for the duration of your appointment.

The University of Cambridge is internationally renowned for its excellence in research and training.

Informal enquiries are welcomed and should be directed to: Mr Adel Helmy [email protected]

Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge, CB2 0QQ UK.

The University values diversity and is committed to equality of opportunity. The University has a responsibility to ensure that all employees are eligible to live and work in the UK.

Fixed-term: The funds for this post are available for 6 months in the first instance.

This appointment requires an Honorary Clinical Contract.

Click the 'Apply' button below to register an account with our recruitment system (if you have not already) and apply online.

Please ensure that you outline how you match the criteria for the post and why you are applying for this role on the online application form.

Please include details of your referees, including email address and phone number, one of which must be your most recent line manager.

Please quote reference ZE41673 on your application and in any correspondence about this vacancy.

The University actively supports equality, diversity and inclusion and encourages applications from all sections of society.

The University has a responsibility to ensure that all employees are eligible to live and work in the UK.

Further information

  • Further Particulars

Stanford University

Clinical Research Coordinator Associate

🔍 school of medicine, stanford, california, united states.

The Stanford Center for Clinical Research (SCCR) is a growing academic research organization within the Stanford Department of Medicine. Our mission is to conduct and promote high-impact, innovative clinical research to improve human health.

At SCCR, we strive to find team members who are passionate about their work, flexible, fun, and want to deliver results. We place a high priority on equipping our staff to perform their job efficiently, helping them acquire new skills and grow within the organization. We encourage our team to have a healthy balance between work commitments and life outside of work and provide support to achieve this balance. If you are looking to make a large impact through global-reaching clinical research, we encourage you to apply!

Duties include:

  • Serve as primary contact with research participants, sponsors, and regulatory agencies.  Coordinate studies from start-up through close-out.
  • Determine eligibility of and gather consent from study participants according to protocol.  Assist in developing recruitment strategies.
  • Coordinate collection of study specimens and processing.
  • Collect and manage patient and laboratory data for clinical research projects.  Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
  • Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed.
  • Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
  • Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
  • Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
  • Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
  • Participate in monitor visits and regulatory audits.

DESIRED QUALIFICATIONS:

  • Bachelor’s degree in a health/medical science or other related field. 
  • Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

EDUCATION & EXPERIENCE (REQUIRED):

  • Two-year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

  • Strong interpersonal skills.
  • Proficiency with Microsoft Office.
  • Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

  • Working toward certification(s) to perform basic patient measurements and tests, such as phlebotomy and EKG.

PHYSICAL REQUIREMENTS:

  • Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
  • Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
  • Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

WORKING CONDITIONS:

  • Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.
  • May require extended or unusual work hours based on research requirements and business needs.

WORKING STANDARDS:

  • Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
  • Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
  • Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University’s Administrative Guide,  http://adminguide.stanford.edu/ .

The expected pay range for this position is $31.73 to $36.54 per hour.

Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.

At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website provides detailed information on Stanford’s extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

Why Stanford is for You Imagine a world without search engines or social platforms. Consider lives saved through first-ever organ transplants and research to cure illnesses. Stanford University has revolutionized the way we live and enrich the world. Supporting this mission is our diverse and dedicated 17,000 staff. We seek talent driven to impact the future of our legacy. Our culture and unique perks empower you with:

  • Freedom to grow . We offer career development programs, tuition reimbursement, or audit a course. Join a TedTalk, film screening, or listen to a renowned author or global leader speak.
  • A caring culture . We provide superb retirement plans, generous time-off, and family care resources.
  • A healthier you . Climb our rock wall, or choose from hundreds of health or fitness classes at our world-class exercise facilities. We also provide excellent health care benefits.
  • Discovery and fun . Stroll through historic sculptures, trails, and museums. 
  • Enviable resources . Enjoy free commuter programs, ridesharing incentives, discounts and more.

The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources at [email protected]. For all other inquiries, please submit a contact form .

Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.

  • Schedule: Full-time
  • Job Code: 1013
  • Employee Status: Regular
  • Requisition ID: 103427
  • Work Arrangement : On Site

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Associate Clinical Research Coordinator - Urology

  • Phoenix, AZ

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Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s). Interacts with various departments within the institution. Works cooperatively with other investigators and personnel at all levels. Interacts with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies.  Position Overview: (Major Functions and Non-Essential Functions):  Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies. Screens, enrolls, and recruits research participants. Coordinates schedules and monitors research activities and subject participation. Recognizes adverse events, protocol deviations, and other unanticipated problems and reports appropriately. Collects, abstracts, and enters research data. Performs administrative and regulatory duties related to the study as assigned. Some travel may be required. ADDENDUM (if applicable) Protocol Development and Maintenance Activities Responsibilities may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes. Participates in other protocol development activities and executes other assignments as warranted and assigned. 

During the selection process you may participate in an OnDemand (pre-recorded) interview that you can complete at your convenience. During the OnDemand interview, a question will appear on your screen, and you will have time to consider each question before responding. You will have the opportunity to re-record your answer to each question – Mayo Clinic will only see the final recording. The complete interview will be reviewed by a Mayo Clinic staff member and you will be notified of next steps.

Minimum Education and/or Experience Required: (Education Requirements and Experience):  HS Diploma with at least 3 years of experience OR Associate's degree/college Diploma/Certificate Program with at least 1 year of experience, Associate’s in Clinical Research from an accredited academic institution without experience OR Bachelor's degree. Experience should be in the clinical setting or related experience.  

Additional Experience and/or Qualifications: (Has Achieved Competency in the Following Areas, Job Knowledge and Additional Considerations):  Graduate or diploma from a study coordinator training program is preferred. One year of clinical research experience is preferred. Medical terminology course is preferred.  Licensure/Certification Required:  N/A 

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PharmaGroww

Clinical Research – Associate

Nagercoil / Kanyakumari

  • Posted 3 hours ago

CapeStart

Website CapeStart

End-to-End Data Annotation, Machine Learning and Software Development for Healthcare, Pharma, SLR, and IT

We’re looking for a proactive and highly communicative clinical research professional, pivotal in critically analyzing and summarizing clinical literature to provide valuable insights. Collaborating with cross-functional teams, you will contribute to the systematic review of medical literature, ensuring that our reports adhere to rigorous standards and regulatory guidelines. Join us in our commitment to excellence within the realm of clinical research and literature analysis.

Research & Analysis

Data Validation

  • Conduct systematic literature reviews (SLR) and meta-analyses, including screening and extraction.
  • Prepare training data for AI model development.
  • Write clinical reports following regulatory guidelines.
  • Ensure data accuracy and quality through thorough checks.
  • Manage assigned projects, meet deadlines, and communicate progress.
  • Summarize articles and create literature summaries.
  • Utilize social media listening to identify patient-reported outcomes.

Any Lifesciences degree, including B. Pharm, D. Pharm, BioMedical Engineering, BioTechnology, Microbiology, etc

0 to 2 Years

To apply for this job please visit www.linkedin.com .

clinical research associate uk jobs

Clinical Research Associate

  • Location: Reading
  • Categories Clinical Monitoring
  • __vacancyopjusttionswidget.opt-Business Area__ ICON Full Service & Corporate Support
  • __vacancyopjusttionswidget.opt-Remote Working __ Hybrid: Office/Remote

Nandhini Selvakumar

Talent Acquisition Sourcing Specialist

  • Full Service Division

Send me a message

About the role, this vacancy has now expired. please see similar roles below....

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Integrity, Collaboration, Agility and Inclusion. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.  

Experienced England, UK-based CRA/clinical research associate required to augment existing non-Oncology CRA team, for pharmaceutical and biotechnology company company partner.

You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

Responsibilities:

  • Contribute to the selection of potential investigators.
  • Provide the required monitoring visit reports within required timelines
  • Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
  • Perform source data verification according to SDV plan and ensure data query resolution
  • Initiate, monitor and close study sites in compliance with client Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.
  • Train, support and advise Investigators and site staff in study related matters.

Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

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A better career. A better world. A better you.

Day in the life

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To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

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How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

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Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

Suzaita Hipolito

Suzaita Hipolito

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    Clinical Research Jobs in United Kingdom. Search and find our latest clinical research jobs based in the United Kingdom. We have jobs available in London and all over the UK, for more information contact us or apply directly to our jobs below.

  21. Clinical Research Associate (Fixed Term)

    The University of Cambridge is internationally renowned for its excellence in research and training. Informal enquiries are welcomed and should be directed to: Mr Adel Helmy [email protected]. Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge, CB2 0QQ UK. The University values diversity and is ...

  22. Clinical Research Associate, UK job in Reading

    About the role. Experienced UK-based Regional CRA/clinical research associate required to augment existing CRA team, for multinational biopharmaceutical company partner. You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies.

  23. 25+ Clinical Research Associate in Dentistry Jobs, Employment in

    Clinical Research Associate (Phase 4, Remote Site Management,Migrain,Neuroscience,TMF,Observational) Tellus Solutions. North Chicago, IL 60064. $43.06 an hour. Full-time + 1.

  24. King's College London hiring Clinical Research Associate I Job in

    Educated to at least A-level or degree level, preferably in a related subject area, e.g. a life science or clinical subject or relevant experience; Sound working knowledge of the prevailing regulations and best research practices pertaining to the conduct of clinical trials, in particular GCP

  25. Clinical Research Coordinator Associate

    Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. ... The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. ...

  26. Search our Job Opportunities at Sanofi

    Search Jobs. Better is out there. Better medications, better outcomes, better science. It's all down to people like you, from different backgrounds, in different locations, doing different roles. Take the most important step in your career: help us change the lives of people, families, and communities for the better.

  27. Clinical Research Associate

    Clinical Research Associate II. ShenYang. ICON Strategic Solutions. Clinical Monitoring. Shortlist. Clinical Research Associate II-Beijing. ICON Strategic Solutions. Shortlist. Experienced England, UK-based CRA/clinical research associate required to augment existing non-Oncology CRA team, for pharmaceutical and biotechnology company...

  28. Associate Clinical Research Coordinator

    HS Diploma with at least 3 years of experience OR Associate's degree/college Diploma/Certificate Program with at least 1 year of experience, Associate's in Clinical Research from an accredited academic institution without experience OR Bachelor's degree. Experience should be in the clinical setting or related experience.

  29. Clinical Research

    Clinical Research - Associate. By Vicky Singh / June 3, 2024. Full Time. Nagercoil / Kanyakumari. Posted 7 hours ago. Website CapeStart. End-to-End Data Annotation, Machine Learning and Software Development for Healthcare, Pharma, SLR, and IT. Job Description. We're looking for a proactive and highly communicative clinical research ...

  30. Clinical Research Associate job in UK, Reading

    Experienced England, UK-based CRA/clinical research associate required to augment existing non-Oncology CRA team, for pharmaceutical and biotechnology company company partner. You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory ...