Clinical trial Work, Jobs in Newmarket, Sfk (with Salaries)

Clinical Trial Coordinator
Thermo Fisher Scientific —Cambridge
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- English
Clinical Research Nurse - GP Surgery based
St Mary's Surgery —Ely
- Part-time
Quick apply
5d
Clinical Trial Coordinator/Clinical Research Nurse
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £32,073 - £39,043 a year
- Full-time
- IT
- Communication skills
Senior Scientist in Molecular Diagnostics for Colorectal Cancer Screening
TOGL (Holdings) Limited —Cambridge
- Full-time
- Doctoral degree
- Laboratory experience
- Master's degree
Quick apply
Healthcare Science Support Worker (Laboratory Assistant)
UK Health Security Agency —Cambridge
- £27,335 - £28,442 a year
- Full-time
- Laboratory experience
- Data entry
22h
Clinical Study Manager
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Project management
- Machine learning
- Annual leave
- Life insurance
Quick apply
Research Governance Administrator
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £25,760 - £27,476 a year
- Full-time
- Microsoft Excel
- Microsoft Office
- Administrative experience
Health, Safety and Facilities Officer
Alzheimer's Research UK —Cambridge
- £32,000 a year
- Communication skills
- Sick pay
13d
Clinical Site Manager
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Management
- Machine learning
- Organisational skills
- Annual leave
- Life insurance
Quick apply
12d
Lead Pharmacist for Clinical Trials, Research, and Innovation
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £57,528 - £64,750 a year
- Full-time
- Master's degree
- Communication skills
- Hospital experience
14d
Policy Campaigns Manager - FTC
Alzheimer's Research UK —Cambridge
- £44,000 a year
- Temporary
- Management
- Continuous improvement
- Leadership
- Sick pay
12d
Senior Clinical Site Manager
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Management
- Laboratory experience
- Machine learning
- Annual leave
- Life insurance
Quick apply
12d
Director, Clinical Safety Scientist (Radiopharmaceuticals)
Bicycle Therapeutics —Cambridge
- Full-time
- Hybrid work
- Leadership
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
Sr Dir Ops - Medical Communications
Thermo Fisher Scientific —Cambridge
- 8 hour shift
- Management
- Doctoral degree
- Leadership
Senior Manager, Regulatory Affairs
Hologic —Cambridge
- £71,000 - £87,000 a year
- Engineering
- Analysis skills
- Leadership
Team Leader - Biostatistics
Bio Pharma Resourcing —Cambridge
- £35,000 - £50,000 a year
- Management
- Doctoral degree
- Master's degree
Executive Director of Clinical Business Development - Strategic Accounts
Syneos Health Commercial Solutions —Cambridge
- Remote
- Sales
- Microsoft Office
- Business development
Executive Director of Clinical Business Development - Strategic Accounts
サイネオス・ヘルス —Cambridge
- Remote
- Sales
- Microsoft Office
- Business development
PCN Senior Clinical Pharmacist
Cam Medical Primary Care Network —Cambridge
- Full-time
- Hybrid work
- Anatomy knowledge
- Medication administration
- Patient care
- Flexitime
Quick apply
13d
General Counsel & Company Secretary (0.8FTE)
Qureight Ltd —Cambridge
- Part-time
- Hybrid work
- Machine learning
- Negotiation
- Annual leave
- Life insurance
Quick apply
2d

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Clinical Trial Coordinator

Thermo Fisher Scientific -
Cambridge

Apply Now

Job details

Full-time

Qualifications

Microsoft Powerpoint
Microsoft Word
Driving Licence
English
Microsoft Office
Bachelor's degree
Driving
Organisational skills
Translation

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.

Position Overview:

As a Clinical Trial Coordinator, you will provide administrative and technical support to the Project Team. You will support audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document.

If you are pursuing a career as a Clinical Research Associate (CRA), consider taking the first step with Thermo Fisher Scientific by applying for the position of Clinical Trial Coordinator. This role offers a valuable opportunity to gain essential experience and develop a strong foundation within the field of clinical research. To be considered for this opportunity, please submit your up-to-date curriculum vitae along with a tailored cover letter. Begin your journey toward a fulfilling career in clinical research today.

Essential Functions:

Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
Ensures allocated tasks are performed on time, within budget and to a high-quality standard. Proactively communicates any risks to project leads.
Supports the maintenance of study specific documentation and systems including but not limited to: study team lists, tracking of project specific training requirements, system access management, and tracking of project level activity plans in appropriate system.
Provides system support (i.e. Activate & eTMF) ).
Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
Supports scheduling of client and/or internal meetings.
Reviews and tracks local regulatory documents.
Transmits documents to client and centralized IRB/IEC.
Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
Maintains vendor trackers.
Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
Assists with study-specific translation materials and translation QC upon request.

Education, Experience and Requirements:

Bachelor's degree or higher in Lifesciences.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).**
Valid driving license for the UK.

** Industry or placement experience preferable.

Knowledge, Skills, Abilities:

Ability to work in a team or independently as required
Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Flexibility to reprioritize workload to meet changing project timelines
Proven ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
Good English language and grammar skills and proficient local language skills as needed
Advanced digital literacy, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
Ability to successfully complete PPD clinical training program
Self-motivated, positive attitude and good interpersonal skills

Why Join Us:

We hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore you will benefit from an award-winning learning and development programme, ensuring you reach your potential.

What we offer:

As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD® clinical research services truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Apply Now

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clinical trial jobs in newmarket, sfk

Clinical Trial Coordinator

Clinical Research Nurse - GP Surgery based

Clinical Trial Coordinator/Clinical Research Nurse

Senior Scientist in Molecular Diagnostics for Colorectal Cancer Screening

Healthcare Science Support Worker (Laboratory Assistant)

Clinical Study Manager

Research Governance Administrator

Health, Safety and Facilities Officer

Clinical Site Manager

Lead Pharmacist for Clinical Trials, Research, and Innovation

Policy Campaigns Manager - FTC

Senior Clinical Site Manager

Director, Clinical Safety Scientist (Radiopharmaceuticals)

Sr Dir Ops - Medical Communications

Senior Manager, Regulatory Affairs

Team Leader - Biostatistics

Executive Director of Clinical Business Development - Strategic Accounts

Executive Director of Clinical Business Development - Strategic Accounts

PCN Senior Clinical Pharmacist

General Counsel & Company Secretary (0.8FTE)

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Education, Experience and Requirements:

Why Join Us:

What we offer:

Apply today! http://jobs.thermofisher.com

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