Clinical Project Manager

Location
Cambridgeshire
Salary
Competitive
Posted
21 Jul 2017
Closes
18 Aug 2017
Ref
J4182
Contact
Eve Hegarty
Contract Type
Permanent
Hours
Full Time
We are currently have a great opportunity available for a Clinical Project Manager to join a growing biotech company based in the Cambridge area. We are looking for an enthusiastic and experienced Clinical Project Manager to join an expanding clinical development team, to manage clinical trials across a growing portfolio of products. You will take responsibility for one or more outsourced clinical studies, working with multi-disciplinary in house teams and CROs to deliver timely and high-quality clinical data.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Clinical Project Manager will be varied however the key duties and responsibilities are as follows:

1. To lead the clinical trial team (internal and external) tasked with delivery of a company sponsored clinical trial.

2. To assist in the selection of appropriate vendors for the conduct of company sponsored clinical trials. You will work with vendors to define operational details of clinical trials.

3. Develop study management plans ensuring sponsor oversight of clinical trials in accordance with company procedures.

4. Review vendor generated clinical trial related documents to ensure compliance with the objectives of the trial, procedures and relevant standards. Ensure essential documents allowing the reconstruction of each trial are generated, filed and maintained.

5. Manage trial budgets and track trial related payments to vendors.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Clinical Project Manager we are looking to identify the following on your profile and past history:

1. Relevant degree in nursing or other healthcare professional equivalent, plus significant experience of managing outsourced clinical trials.

2. Experience in clinical trials across a range of therapeutic areas and geographies, preferably with substantial Oncology experience. Knowledge of GCP and related regulatory guidelines governing clinical trials in the UK, EU & USA.

3. Excellent matrix management skills and ability to manage contractors and collaborators, with the ability to see complex projects to completion, and to work on a broad range of tasks within a project.

Key Words: Clinical Project Manager | Clinical Trials | GCP | Clinical Research Organisation | CRO | Oncology

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.