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Job Details

Clinical Project Manager

Company: Key People Limited
Location: Prague
Reference: mc 23769
Closing Date: 20 Dec 18
Type: Permanent
Salary (£): 30,000 - 40,000
Benefits:

Job Summary:

Our leading pharmaceutical client is looking for a Clinical Project Manager to work on global studies.The successful candidate will be responsible for clinical execution and management of all aspects of assigned clinical studies (interventional and non-interventional, from early phase to late phase) and managed access programs (MAP) executed by PLS on behalf of Novartis Organizations, under the lead of Senior Clinical Project Manager.Responsibilities1. ...

Requirements:

Our leading pharmaceutical client is looking for a Clinical Project Manager to work on global studies.

The successful candidate will be responsible for clinical execution and management of all aspects of assigned clinical studies (interventional and non-interventional, from early phase to late phase) and managed access programs (MAP) executed by PLS on behalf of Novartis Organizations, under the lead of Senior Clinical Project Manager.

Responsibilities

1. Agree with customer team and Line Functions on realistic project and study timelines. Esca-late to higher level in the organization if no agreement can be achieved or support the Sr. CPM.

2. Lead and manage a multidisciplinary cross functional Clinical Trial Team (CTT) (medical writing, statistics, data management, monitoring partner, drug supply, regulatory, safety etc.) or support the Sr. CPM (where applicable) in the effective planning, regular re-evaluation and implementation of assigned clinical studies and MAP/PTA/IIT programs according to Novartis Global processes ensuring adherence to timelines, budget, quality standards and operational procedures.

3. Responsible for investigators meeting organization and all internal meetings related to the clinical trial execution and operational excellence

4. As applicable, directly interact with investigator sites and CRAs/CROs/vendors to ensure smooth study set up and smooth study conduct, reviewing site performance, protocol deviations, ongoing risk assessment and timely issue resolution in alignment with Novartis global standard with local regulation requirement.

5. In collaboration with the Sr.CPM (as applicable) support compilation of study regulatory documents for submissions to competent authorities and ethics-committees in collaboration with other associated PLS, Novartis line functions and CRO Partners as required. Also if needed support clinical studies with all onsite/remote monitoring activities and communications with investigators, investigational sites, clinical trial team, healthcare professional and other associated internal line-functions.


Key People is a specialist international recruitment consultancy with over 25 years’ experience of working within the life sciences, biotech, healthcare and CRO industries. Our experienced and dedicated clinical research related consultants have a long history of success, excellent technical knowledge and a flexible, consultative focussed approach to recruitment.

Please contact Mark Cussens, Clinical Research Recruiter on
Tel: +44 1727 817623 or email: mcussens@keypeople.co.uk
Tel: +41 4350 86620 or email: mark.cussens@keypeopleswitzerland.ch

Key People is a recruitment company with a reputation for providing good value that’s been built up over 20 years.
- We achieve results faster
- Our candidates really are a cut above
- We add greater value
We think it’s because we’re a private company driven by clients, not by shareholders.

For our candidates, we have developed relationships with thousands of clients nationwide and across Europe, who choose to recruit through Key People, so you’ll have a wide choice of opportunities to further your career.

Apply for this job: Clinical Project Manager

Contact Information:

Address:  Head Office
Catherine House
Adelaide Street
St Albans
Hertfordshire
AL3 5BA
England
Tel:  Tel: 44 (0) 1727 811634
Fax:  Fax: 44 (0) 1727 844838
Website:  Visit Our Web Site

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