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Job Details

Clinical Study Manager in Warsaw

Company: SEC Recruitment
Location: Poland
Reference: PP-POL-1234
Closing Date: 16 Aug 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

My client, global pharmaceutical company with an impressive pipeline is seeking an Clinical Study Manager to join their Study Management team and cover the CEE region on a permanent basis. This is permanent office based role in Warsaw with flexibility working from home.Role and responsibilities:• Providing leadership and local strategic planning and organisation to ensure delivery of the operational aspects of the study management. ...

Requirements:

My client, global pharmaceutical company with an impressive pipeline is seeking an Clinical Study Manager to join their Study Management team and cover the CEE region on a permanent basis. This is permanent office based role in Warsaw with flexibility working from home.

Role and responsibilities:
• Providing leadership and local strategic planning and organisation to ensure delivery of the operational aspects of the study management.
• Responsibility for all assigned studies at the regional level including compliance to timelines, budget, quality standards (ICH/GCP/GPP) and other local requirements.
• Leadership and active participation in preparation level of the study – especially in start-up phase. Management of work of the local research teams as well as external vendors.
• Accountability for achieving patient recruitment targets, timelines, managing study patient recruitment strategies.
• Responsibility for development and oversight of the local study budget on the regional level.
• Leadership the local study team to reach study goals.
• Planning and oversight of the scope of work on the regional level – ensuring monitoring activities are performed in accordance with study TMP and reports are timely.
• Ensuring allocated studies are completed in accordance with pre-defined budget and timelines.

Required skills and qualifications:

As a potentially successful applicant you must have at least 4 years of monitoring experience, preferably as Lead CRA. You should also have a minimum of a Bachelor’s Degree in a life science and extensive knowledge of ICH – GCP and other regulatory requirements as well as a strong understanding of the various aspects of clinical trials (clinical monitoring, clinical data management, regulatory compliance etc). You must be able to communicate very clearly and accurately in written and spoken Polish, possess leadership and negotiations skills.
Candidates with a CRO or pharmaceutical company background will both be considered for this position.

This is a fantastic opportunity to work for a pharmaceutical company currently enjoying strong success in a number of therapeutic areas. For the right candidate the organisation is happy to offer excellent salary, great additional benefits package and flexibility to work home-based.

To apply for this role please send your CV to Paulina.Piesta@secpharma.com or call +44 (0) 207 255 6665 for more information.

Apply for this job: Clinical Study Manager in Warsaw

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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