Enable job alerts via email!

Clinical Trial Manager

CK Group- Science, Clinical and Technical

London

Hybrid

17 days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player is seeking a Clinical Project Manager to oversee clinical trials in a hybrid role. This position involves managing budgets, ensuring data integrity, and collaborating with stakeholders to maintain compliance with regulatory standards. The ideal candidate will have over 5 years of clinical trial management experience, strong analytical skills, and a solid understanding of safety and ethics in the life sciences sector. Join a forward-thinking company that leverages artificial intelligence to optimize research outcomes and make a significant impact in the industry.

Qualifications

  • Strong knowledge of safety and ethics in clinical trials.
  • Experience in managing budgets and resources effectively.

Responsibilities

  • Oversee budget and resources for clinical trials.
  • Ensure integrity and accuracy of clinical trial data.
  • Liaise with stakeholders and provide updates on study progress.

Skills

Budgeting and tracking

Safety and ethics knowledge

Site management coordination

Clinical trial management

Analytical skills

Education

5+ years of experience in clinical trial management

Job description

CK Group are recruiting for a Clinical Project Manager, to join a leading provider of advanced analytics research and technology solutions to the life sciences industry, at their site based in Paddington, London, Basildon, and working from home, on a contract basis for 12 months.

This role is a hybrid position.

Rate:

£30.08 per hour PAYE.

Clinical Project Manager Role:

  1. Overseeing the budget for clinical trials and ensuring that resources are allocated appropriately. Including managing staff, equipment, and supplies, as well as monitoring expenses and identifying cost-saving measures.
  2. Recruiting, training, and supervising vendor/staff, including clinical research associates and data managers. Ensure that vendor/staff are properly trained on study protocols and that they follow GCP guidelines and other regulatory requirements.
  3. Ensuring the integrity and accuracy of clinical trial data by overseeing data management activities, including data collection, analysis, and reporting as well as ensuring that data is stored securely and in compliance with regulatory requirements.
  4. Developing and implementing quality control measures to ensure compliance with regulatory requirements and standards.
  5. Liaising with study CROs, principal investigators, and other stakeholders to provide regular updates on study progress and to address any issues or concerns that arise during the course of the study.

Your Background:

  1. Knowledge of budgeting and tracking.
  2. Strong knowledge of safety and ethics.
  3. Ability to coordinate site management with research activities.
  4. Experience within outsourcing and contracts within the Pharmaceutical industry is preferred or at least demonstrable knowledge of contracts, bid meetings and negotiations.
  5. Minimum 5+ years of experience in clinical trial management.
  6. Detail-oriented, analytical, and able to work effectively in a team environment.

Company:

Our client offers research services and technology solutions in the life sciences industry. With just under 100,000 employees, the company has operations in over 90 countries worldwide. Our client's ambitions involve optimising results of innovations using artificial intelligence. They believe in utilising data collected to the maximum rather than focussing on gathering lots of information: they use artificial intelligence to do this.

Location:

This role is a hybrid role, it is based at our client's site in Paddington, London and also Basildon.

Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

Please note:

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.

Similar jobs

Senior Clinical Trials Manager

Only for registered members

London

On-site

GBP 45,000 - 85,000

Today
Be an early applicant

Clinical Trial Manager

Only for registered members

Greater London

Hybrid

GBP 40,000 - 80,000

3 days ago
Be an early applicant

Clinical Trial Manager

Only for registered members

London

On-site

GBP 50,000 - 90,000

3 days ago
Be an early applicant

Clinical Trial Manager

Only for registered members

London

On-site

GBP 50,000 - 90,000

7 days ago
Be an early applicant

Senior Clinical Trials Manager

Only for registered members

London

On-site

GBP 50,000 - 90,000

3 days ago
Be an early applicant

Associate Clinical Trial Manager (PhD) - Cardiovascular

Only for registered members

London

On-site

GBP 35,000 - 55,000

8 days ago

Clinical Trial Manager UK, In Vitro Diagnostics

Only for registered members

Maidenhead

On-site

GBP 40,000 - 80,000

4 days ago
Be an early applicant

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology

Only for registered members

London

On-site

GBP 30,000 - 60,000

8 days ago

Associate Clinical Trial Manager (PhD) - Gastrointestinal

Only for registered members

London

On-site

GBP 35,000 - 65,000

8 days ago