Senior Clinical Project Manager
- Employer
- Warman O’Brien
- Location
- London (Central), London (Greater) (GB)
- Salary
- Competitive Annual Salary plus Bonus and Benefits
- Start date
- 23 Sep 2021
- Closing date
- 23 Oct 2021
View more
- Discipline
- Clinical Research, Clinical Project Manager
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Working with a global oncology biotech, as a Senior Clinical Project Manager you will responsible for coordinating and managing allocated studies. This position will be based in London, with a requirement to be on-site in their corporate HQ.
Key Responsibilities will include:
- Be responsible for the overall efficient day-to-day clinical trial management of studies (Set-up to close- out, including the review of all Serious Adverse Events, ensuring medical review and reporting requirements are met)
- Play a pivotal role in our Clinical Operations team leading clinical studies within a programme.
- Act as an expert in your therapy area, working independently with guidance when appropriate.
- Serve as a close partner to the study physicians, assisting in coordinating the activity of research team and holding accountability for projects
- This position will have key relationships with internal stakeholders within the clinical project team, as well as externally with KOLs, investigators and external service providers
- Assist in the development and design of studies to determine the scientific viability of a particular cell product and interpret the results of these studies
- Review and interpret medical data and clinical trial data, draw conclusions, and potentially identify new research and development opportunities
- Perform occasional interim monitoring visits, including site qualification, initiation, and close-out. Including the source data verification of CRFs and Data clarification forms as stipulated.
Requirements of the Role:
- Prior experience as a Senior Clinical Project Manager
- Experience within oncology, preferably Early Phase Trials
- Previous experience of site monitoring in oncology studies
- Excellent communication and interpersonal skills
- Knowledge of ICH-GCP guidelines, EU directives and FDA regulations
- Effective problem-solving skills
- Attention to detail and timelines
What this role can offer you:
- An excellent opportunity to progress within a fast-paced biotech
- A competitive basic salary plus bonus and benefits
- Long-term opportunities for career progression and growth
Company
Warman O’Brien is a global specialist Life Sciences Recruitment Partner across the UK, Europe, USA and APAC. We recruit top talent across a number of functional areas including:
- Biometrics
- Data Sciences
- Quality Assurance
- Regulatory Affairs
- Clinical Research
- Discovery Sciences
- C-Suite
- Medical Affairs
We cover contract and permanent vacancies, executive search, and SOW for companies across the pharmaceutical industry.
Find out more on our website warmanobrien.com/
- Website
- https://warmanobrien.com/
- Telephone
- +44 (0) 2033255075
- Location
-
Floor 5
Regal House
70 LONDON ROAD
Twickenham
TW1 3QS
United Kingdom
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert