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UK CRA Jobs
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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
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Senior Clinical Research Associate
- United Kingdom
- Competitive
We are currently looking for a Senior Clinical Research Associate (SCRA) to join our Clinical Operations Team in the UK. This role can be office-b...
View details Senior Clinical Research Associate
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Parexel are currently recruiting for an Senior Clinical Research Associate, to cover UK sites. In this role, the Senior Clinical Research Associate...
Lead Clinical Research Associate - Europe
- Homeworking, Delaware, United Kingdom
- United BioSource Corporation.
UBC are currently recruiting within our clinical leadership team, we are looking to recruit a Lead CRA within the EU. UBC are a leading provider of
View details Lead Clinical Research Associate - Europe
- 17 days ago
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Senior Clinical Research Associate (CRA) - UK - Home-based
- Worldwide Clinical Trials
Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology
View details Senior Clinical Research Associate (CRA) - UK - Home-based
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CRA II / Senior CRA - 1 year FTC - Sponsor Dedicated - Liver and Alzheimer's Disease - Travel in Wes
- Syneos Health
Senior Clinical Research Associate I Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate cust...
View details CRA II / Senior CRA - 1 year FTC - Sponsor Dedicated - Liver and Alzheimer's Disease - Travel in Wes
- 5 days left
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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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Clinical Research Associate - Oncology
- United Kingdom, Homeworking
- ICON Strategic Solutions
Experienced, high-performing (Midlands/Northern England), UK-based CRA/clinical research associate required to augment existing Oncology CRA team, for
View details Clinical Research Associate - Oncology
- 12 days ago
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Clinical Research Associate - 1 year monitoring required
Role: Clinical Research Associate Location: South West of the UK (Swansea, Cardiff, Swindon, Bristol and Southampton) Fully sponsor dedicated
View details Clinical Research Associate - 1 year monitoring required
- 18 days ago
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Senior CRA - FSP
- £45,000 - £60,000 (depending on experience)
- RBW Consulting
🔍 FSP CRA OPPORTUNITIES WITHIN PHARMACEUTICAL AND BIOTECH COMPANIES Are you looking for a Clinical Research Associate role that can increase the...
View details Senior CRA - FSP
- 11 days ago
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CRA - Sponsor Dedicated
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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Senior CRA / CRA II
View details Senior CRA / CRA II
- 15 days ago
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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.
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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Clinical Research Associate (Sponsor Dedicated) 2024
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
- Balancing sponsor generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs
You will need
- 18 months+ of monitoring experience in phase I-III trials as a CRA
- College degree in medicine, science, or equivalent
- Previous monitoring experience in medium-sized studies, including study start-up and close-out
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
- Excellent written and verbal communication
- Ability to work to tight deadlines
- Availability to travel (fly and drive) and should possess a valid driving license
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. 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, colour, 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 through the form below.
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Clinical Research Associate, UK
- Location: Reading
- __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
- Categories Clinical Trial Management
About the role
This vacancy has now expired. please see similar roles below....
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. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.
Amongst other tasks, your main responsibilities will be to;
- 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.
Strong experience (~>2 years') working as a UK clinical research monitor (or CRA), and already residing within the UK (with appropriate right-to-work in the UK already granted, if applicable)
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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.
Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high stan
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ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
2024-109199
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2024-109201
2024-108424
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ICON Full Service & Corporate Support
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
As a Clinical Trial Manager you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions.
2023-103323
Office Based
2023-101501
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Clinical Research Analyst
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Senior Clinical Research Associate jobs. Clinical Trial Specialist jobs. More searches. Today's top 424 Clinical Research Associate jobs in United Kingdom. Leverage your professional network, and get hired. New Clinical Research Associate jobs added daily.
Clinical Research Associate. ICON. London. Good knowledge of concepts of clinical research and drug development. ICON plc is a world-leading healthcare intelligence and clinical research organization. Posted. Posted 12 days ago ·. More... View all ICON jobs - London jobs.
Search Clinical research associate jobs. Get the right Clinical research associate job with company ratings & salaries. 181 open jobs for Clinical research associate. ... For those with medical and/or health/life science interest and background who want to explore the research field, travel the UK, and be part of a team bringing pharmaceutical ...
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Current Informatics Analyst in London, England, England. Private health insurance, free on site gym membership, hybrid after 6 months of employment. Search Clinical research associate jobs in United Kingdom with company ratings & salaries. 191 open jobs for Clinical research associate in United Kingdom.
Role: Clinical Research Associate Location: South West of the UK Fully sponsor dedicated ICON plc is a world-leading healthcare intelligence and clinical… Posted Posted 30+ days ago · More... View all ICON jobs - London jobs - Clinical Research Associate jobs in London
New Works. Contract, full-time. CK Group are recruiting for a Global Study Associate Director to join a company in the Pharmaceutical industry working remotely initially on a contract basis for 12 months. Daily Rate: 477.00- 577.00 Ltd/Umb (Outside IR35) Global Study Associate Dire... Go to similar: Director jobs.
Contract Clinical Research Associate jobs. Senior Clinical Research Associate jobs. Clinical Trial Specialist jobs. Today's top 99 Clinical Research Associate jobs in London, England, United Kingdom. Leverage your professional network, and get hired. New Clinical Research Associate jobs added daily.
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You will need a passion for oncology. UK clinical research jobs (CRA Jobs). CRA (clinical research associate) jobs from major clinical research organisations across the world. Specialist Clinical Research Associate. Senior 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.
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ICON Strategic Solutions. Clinical Monitoring. Clinical Trial Associate (CTA) Warsaw. Reading. ICON Full Service & Corporate Support. Clinical Trial Support. Read more. Global Clinical Trial Manager.
Contact: Recruitment Team. Reference: Totaljobs/ORA-215724. Job ID: 102044586. Apply. View details and apply for this clinical research associate job in UK with Oracle on Totaljobs. Job Description Cerner Enviza is a leading global healthcare consulting firm and trusted advisor to many of the world's top pharmaceutical, biotech, and medical ...
Apply for Senior / Clinical Research Associate - UK job with Thermo Fisher Scientific in Remote, United Kingdom. Clinical Research jobs at Thermo Fisher Scientific
The Newcastle University-CRUK Clinical Academic Training (NU-CAT) programme offers fully funded 3 year PhD fellowships for clinicians wishing to develop an academic career in cancer research. The training programme is integrated in the NIHR NHIP Academy, benefitting from the mentoring and support available during PhD studies and beyond to build ...
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Clinical Research Associate (Sponsor Dedicated) 2024. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
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Clinical research jobs; Freelance Clinical Research Associate (CRA) - UK; Freelance Clinical Research Associate (CRA) - UK AKRN Scientific Consulting. United Kingdom. Job description. JOB SUMMARY. This is a Freelance position (0,2 - 0,8FTE) for a clinical trial project based in the UK. Under the direction of the Director of Clinical Operations ...
1,007 Clinical research jobs in United Kingdom. Most relevant. Medpace, Inc. 3.3. Entry Level - Clinical Research Associate. London, England. GBP 40K - GBP 56K (Glassdoor Est.) Must hold a valid drivers licence. Hybrid work-from-home options (dependent upon position and level).
Quick Questions with a Clinical Research Associate Play a game of pickleball with Nisha Shah to get a glimpse into work and life as a CRA at IQVIA. Learn More January 30, 2024 3 minute read Blog Careers Related Content Blog - Featured Related Content - CRA Related Content - Clinical Research
Name: Andreia Wendt Position: Postdoc Research Associate Company: Wellcome Centre for Integrative Parasitology, University of Glasgow I'm responsible for… Pursuing academic research, focused ...
Today's top 29,000+ Clinical Research jobs in United Kingdom. Leverage your professional network, and get hired. New Clinical Research jobs added daily. ... Associate (521) Mid-Senior level (6,345) Director (343) Done On-site/remote On-site (27,277) Remote (1,162) Hybrid (1,056) Done Be the first to hear ...
Pharmacovigilance Project Manager. Location: UK (Note: homebased or hybrid working)ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
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.
Job Summary : The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research ...
We help connect talent and opportunities. We are currently hiring for our client who is one of the leading global providers of advanced analytics, technology solutions, and clinical research ...
The Department of Family and Community Medicine seeks a Senior Research Associate to join our team! First, the Senior Research Associate will join research directed by Dr. Nora Gimpel to explore community health outcomes through Student-Run Free Clinics. Data collection to measure success of the programs, such as the number of students ...
Apply for Associate Optimization Specialist job with Thermo Fisher Scientific in Taguig City, Philippines. Clinical Research jobs at Thermo Fisher Scientific