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Job Details

Project Data Manager

Company: SEC Recruitment
Location: Cambridge
Reference: BBBH110970
Closing Date: 27 Feb 18
Type: Permanent
Salary (£): 40,000 - 60,000
Benefits: Amazing Flexible Benefits

Job Summary:

A international Pharmaceutical company, based in Cambridge, is offering a rare opportunity to join the Clinical DM team as a Project Data Manager. In this oversight role, your primary function will be to serve as the DM study expert, providing oversight on all outsourced studies under your remit. The purpose of your role is to ensure consistent delivery of quality data in a timely fashion.

Requirements:

Oversight Project Data Manager – Pharmaceutical – Cambridge – Competitive salary and excellent benefits flexibility programme

If you would like to learn more about this job or any other CDM opportunities please reach out to Eleni or Mark on +44 (0) 207 255 6665 or mark.wilkins@secpharma.com eleni.boumpa@secpharma.com

A international Pharmaceutical company, based in Cambridge, is offering a rare opportunity to join the Clinical DM team as a Project Data Manager. In this oversight role, your primary function will be to serve as the DM study expert, providing oversight on all outsourced studies under your remit. The purpose of your role is to ensure consistent delivery of quality data in a timely fashion.

This is a cross functional role, and this company is focused on finding a candidate who is a confident communicator, capable decision maker, problem solver and works well under pressured timelines. You will lead the vendor CRO through challenges and provide effective guidance to ensure the quality standards are met, on budget and on time.

The key skills we are looking for technically are;

- Several years of Study leadership in either a Pharma or CRO setting – preferably with both
- Strong experience working with outsourced vendors – several years would be required to impress the line manager
- Budgeting experience
- Capable of reviewing sensitive study documents and providing guidance and feedback on interpretations of protocols and procedures.
- Comfortable communicator in all areas – this would include the ability to resolves difficult situations and conflicts.
- Full cycle study experience from Protocol review to Archiving
- SOP improvement experience

Technical Experience requirements

- EDC – Medidata RAVE
- Any experience with electronic diaries, ePRO or eDiary
- Data Visualisation tools – SpotFire, Comprehend – not essential experience but certainly preferred
- Life Science degree or equivalent experience in the life science industry.

This role will be office based in Cambridge. You must currently have the right to work in the UK and no sponsorship will be provided.

If you would like to learn more about this job or any other CDM opportunities please reach out to Eleni or Mark on +44 (0) 207 255 6665 or mark.wilkins@secpharma.com eleni.boumpa@secpharma.com

Apply for this job: Project Data Manager

Contact Information:

Address:  Head Office
3rd Floor, 13-15 Moorgate London.
EC2R 6AD
England
Tel:  00 44 (0) 207 255 6600
Fax:  00 44 (0) 1483 888997
Website:  Visit Our Web Site

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