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Job Details

Clinical Project Manager – Small Pharmaceutical – France – Diabetes - €70,000

Company: Barrington James Clinical
Location:
Reference: zcbd-1989-fradia12
Closing Date: 21 Dec 16
Type: Full Time
Salary (£): 60,000 - 80,000
Benefits:

Job Summary:

I am currently representing a small/mid-sized specialist pharmaceutical in France, developing products in type I and II diabetes. Due to strong financial backing and an expanding pre-clinical portfolio, my client is now seeking an experienced clinical project manager to lead phase II and III projects, with a particular emphasis on US trials.

Requirements:

Clinical Project Manager – Small Pharmaceutical – France – Diabetes - €70,000

 

I am currently representing a small/mid-sized specialist pharmaceutical in France, developing products in type I and II diabetes. Due to strong financial backing and an expanding pre-clinical portfolio, my client is now seeking an experienced clinical project manager to lead phase II and III projects, with a particular emphasis on US trials.

 

BACKROUND

Details confidential, more available upon application. Exciting company in France with a real scientific passion for the development of diabetes programmes. They have their own in-house development portfolio as well as partnering with a number of research institutes across Europe.  Reporting to the Director of Clinical Research, you’ll have full control of project metrics, timelines and development goals across Europe.

 

PRIMARY DUTIES 

Seeking an experienced Clinical Project Manager to lead oncology projects phases I – III in an exciting specialist French biopharmaceutical.

 

Identifies project guidelines and communication needs by:

- Reviewing study requirements and response assessment criteria and collaborates with key stakeholders to develop study start-up activities and associated documents

- Establishing clear and measurable project operating guidelines with Director of Clinical Research and relevant representatives

- Defining project plans (i.e. timelines, milestones and limitations for project staff)

- Establishing project reporting schedules with Director of Clinical Research and relevant representatives

- Providing project updates to Director of Clinical Research and relevant representatives on schedule

- Communicating timely, appropriate project information to project teams, sites and company/sponsor representative(s)


Performs project analysis and management by:

- Identifying critical project success factors for tracking, analysis and reporting

- Determining needed resources for project completion and communicating needs to appropriate departmental managers

- Collaborating with department leaders for appropriate training of those involved with the project toward excellence in successful and timely completion of project

- Developing budget and expense review strategy

- Creating proactive cost containment strategies and communicating them to project team

- Reviewing regularly the task/time budget and expenses with team

- Understanding SOPs and working closely with QA for clarification and documentation of deviations

- Training and maintaining project team knowledge and applications of SOPs

- Communicating all protocol clarifications/revisions to project team

- Coordinating site management of data collection with internal and external teams

- Possessing a thorough understanding of the project contract and totals needed for monthly revenue reporting

- Managing pass through expenses associated with the project



Oversees project close out by:

- Assisting with coordination of submission activities, as applicable

- Assisting with initiating and overseeing all project close out activities to completion

 

 

Required Skills:

- Strong interpersonal and communication skills, both verbal and written

- Strong organizational and leadership skills

- Goal oriented

- Ability to maintain professional and positive attitude



Required Experience:

- Lifescience degree

- Previous management or project experience in clinical development of diabetes beneficial

- 5yrs + years clinical trials or project management experience within a CRO or pharmaceutical research organization required; preferably in a project management related role

- Working knowledge of GCH, ICH guidelines and FDA regulations

- Experience working with computer software including Word, Excel, Access and Project preferred

 

Want to find out more and APPLY NOW?

To find out more about this and other exciting opportunities based in the UK and Europe then please contact Zac Beda now for an informal and confidential chat about industry possibilities.

zbeda “at” barringtonjames dot com

 

Keywords:

Project manager | consultant | clinical research | senior project manager | freelance | contract | interim | freelancer | CRO | pharma | biotech | clinical project manager | project management | clinical trials | Diabetes | type 1 | type 2 | type II | Type I Gene | Gene Therapy | Therapy | Rare | Disease | Rare Disease | Stem | Cell | Stem Cell | Oncology | Cancer | Diabetes | Immunology | Europe | Office based | Home based | UK | United Kingdom | London | Scotland | Glasgow | Edinburgh | Wales | Cardiff | France | Paris | Lille | Marseille | Geneva | Switzerland | Nice | Lyon

Apply for this job: Clinical Project Manager – Small Pharmaceutical – France – Diabetes - €70,000

Contact Information:

Address:  Head Office
Victoria House
Consort Way
Horley
Surrey
RH6 7AF
England
Tel:  01293 776644
Fax:  01293 822333

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