This job has expired

Senior Clinical Operations Manager

CK Group
Closing date
19 Feb 2022

View more

Contract Type
Full Time
You need to sign in or create an account to save a job.

Job Details

CK Clinical are recruiting for a Senior Clinical Operations Manager to join a Global Pharmaceutical Company at their site based in Central London on a permanent basis.

Senior Clinical Operations Manager Role:
The main purpose of the role will be to have a high level of oversight and manage clinical trials across a number of therapeutic areas. This may either be directly or through providing leadership in managing/directing the internal/external study team members. The role holder will be fully accountable for ensuring that the timeline, budget, quality and integrity of clinical trials is consistent with the clinical study protocols and other study requirements.

Responsibilities will include to:
- Oversee, supervise, mentor and assist clinical operations, when required, to ensure adherence to agreed project plan, budget, and quality specifications for individual clinical trials.
- Be the primary contact for all study operational management related communications, including for managing/answering questions related to trial procedures and patients' eligibility.
- Monitor and report the study progress and quality, analysing potential issues and risks, and escalating/resolving them as appropriate.
- Monitor, assess and report on their performance and quality of work (especially to ensure that CRAs are monitoring the study as expected).
- Provide input to study documents, including e.g., but not limited to, study protocol, statistical analysis plan, clinical study report, audit plan, and/or author relevant sections of study documents.
- Organise and chair the monthly project meeting(s).
- Organise study meetings/training as required.

Your Background:
- Minimum BSc in the Life Sciences, Nursing degree, or equivalent combination of education and experience.
- Significant demonstrable clinical research experience gained within a contract research organisation (CRO), pharmaceutical, or Biotechnology Company, with proven experience of technical and/or project management in conducting multi-national and/or single site early phase clinical trials in a pharmaceutical company or CRO.
- Thorough knowledge of regulatory requirements, clinical development, and clinical monitoring procedures.
- Demonstrable experience of leading project/study teams.
- Ability to oversee and manage CROs throughout the entire clinical operations life cycle of a study.
- Flexibility and the ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.

Entitlement to work in the UK is essential. For more information or to apply for this Global Clinical Operations Leader position, please contact Jim Gleeson on 01438 842973 or email Please quote reference 52357.


Find the career you always dreamed of

We are the CK Group, the UK’s specialist in scientific, clinical and technical recruitment.

We have 4 brands:  

  • CK Science is the leading independent scientific recruitment consultancy.
  • CK Clinical is an established leader in the clinical research and drug development sectors
  • CK Technical specialises in jobs for Engineers and IT professionals
  • CK QLS finds roles for high calibre professionals working in the science and technology sectors in Switzerland.

Over the last 28 years we have found jobs for thousands of high calibre scientists in the scientific, chemical, waste, biotechnology and pharmaceutical industries. By working with us to find your next job, you will get access to the best scientific vacancies in the UK, Europe and the rest of the world.

We are proud to be working with 18 out of the world’s top 20 scientific organisations.

We can help you find your dream job.

Find Us
+44 (0)1246 457700
CK Group
Westwick House
The Bridge Business Centre
Beresford Way
S41 9FG
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert