Clinical Project Manager - Oncology

inVentiv Health Clinical
45, 000-55, 000
02 Dec 2017
07 Jan 2018
Contract Type
Full Time
Clinical Project Manager
Office based in Surrey - flexibility to working from home


Here at INC Research/inVentiv Health Clinical we are currently recruiting for a Clinical Project Manager (Local Oncology studies) to be based in Surrey (with some flexible home working on offer).

Job Details:

Here at INC Research/inVentiv Health Clinical we are recruiting for a Clinical Project Manager to be based with one of our global pharmaceutical clients.

This is an opportunity to play your role in contributing to the success of Oncology studies. In this post you will take lead of UK trials to ensure objectives are met within timelines and budget. Provide a central point of communication between global teams and director and lead trial teams.

- Provides a central point for communication between Global, Regional and UK Trial Team for delivery and management of Oncology trials according to timelines, budget and performance metrics.
- Directs and leads the UK Trial Team, cascades milestones to ensure trials undertaken meet or exceed targets.
- Monitors trial resource requirements, working with the CRA Manager to ensure trials are resourced appropriately.
- Drives Feasibility Review to evaluate new trials and coordinates feedback to the UK Medical Director and Country Head.
- Leads centre selection in conjunction with CRAs, Medical Scientific Liaison functions and selects appropriate sites.
- Provides protocol specific training to CRAs and supports with evaluation visits as required.
- Coordinates and attends investigator meetings as required.
- Writes and coordinates MREC submissions and attends MREC meetings as required.
- Accountable for ensuring distribution of all safety updates to investigators and MRECs.
- Communicates clearly with regulatory department regarding local regulatory submissions for CTAs.
- Completes Trial Commitment Forms assuring best outcome according to metrics and approves budget allocation.
- Negotiates contracts with CROs, SMOs and NHS Trusts as required.
- Management of the country level TMF and the creation and signoff of the Country level Table of Contents.
- Develops recruitment strategies and contingencies in conjunction with CRAs and Medical Team.
- Contributes to the design/writing of UK trial protocol, reports and publications where required and within agreed timelines and budget.
- Ensures local Phase IV studies are posted on the appropriate Registration and public databases.
- Develops and maintains relationships with KOLs and investigators.
- Completes Site Specific Worksheets (SSWs) for globally outsourced studies and is the main point of contact for the global team and CRO regarding UK management.


To be eligible candidates should have:

* Bachelor's Degree (or equivalent) or MSc or PhD.
At least 5 years UK clinical research experience
* Experience in UK clinical trial management of Oncology Phases I to IV
* Significant experience in managing clinical research studies, clinical operations or equivalent
* In depth knowledge of GCP's and ICH guidelines
* Excellent communication and leadership skills.


There are many benefits available to employees of INC Research/inVentiv. They include highly competitive compensation and benefits including: 25 days annual leave, sick pay, contributory pension, private healthcare, dental plan, life assurance, childcare vouchers, business travel insurance and personal accident policy management support / career counseling and bonuses!

Application Details

If you have the required experience for this position and are eligible to work in the UK then please apply by CV.

To find out more about our company and search and apply for other open jobs please visit our website *************************************

Please be aware that due to the volume of applications received, only applicants being considered for this job opening will be contacted for further discussions.

"Join an industry-changing company that is reinventing the way we develop and commercialize drugs. At INC Research/inVentiv Health our 22,000 employees have one purpose: shortening the distance from lab to life. You'll work alongside the brightest minds to create better, faster, smarter processes to speed therapies to patients that need them the most. In fact, in a recent five-year period, INC Research/inVentiv Health has helped to develop or commercialize at least 82% of novel new drugs approved by the FDA and at least 70% of products granted marketing authorization by the EMA."