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Job Details

Clinical Study Manager

Company: Docs Global (Continental Europe)
Location: Solna,Sweden
Reference: Ref AS-024514
Closing Date: 22 Mar 18
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

Why Apply This position is with an innovative Biopharmaceutical company, which is known for their innovative and market leading products, a stable workforce and a positive company culture. To express your interest and to find out more about the role, please send your CV today to Claudia.JorgensenRankine@docsglobal.com. *Applicants who have not had a response within two weeks should assume their application has been unsuccessful.

Requirements:

Roles & Responsibilities of the position

Roles & Responsibilities of the position include

- Overall responsibility to lead, manage and deliver clinical programs for development projects as well as marketed products
- Ensure that a clinical program strategy is developed and implemented in accordance with the
- overall therapeutic area strategy, project/product goals and regulatory requirements
- Coordinates, contributes to and ensures delivery of key clinical study documents such as study protocols, protocol amendments, case report forms, patient information documents and clinical study reports as well as project management plans
- Defines the scope for ESPs, lead and manage appointed ESPs, and follow-up on ESP performance
- forecasts and manages resources, budget and timelines for individual clinical studies and ensures that all clinical study activities and deliverables are compliant with the client’s SOPs, ICH/GCP guidelines and regulatory requirements

Job Requirements

Job Requirements

- University degree in Life/Health Sciences
- A minimum of 5 years’ experience of planning, conducting and reporting multicenter, international clinical studies
- Extensive knowledge of all aspects of the clinical study process
- Experience of managing ESPs
- Demonstrated ability to lead multi-disciplinary teams including team building, negotiation and conflict resolution
- Excellent written and oral communication skills in English & Swedish

Personal attributes

• A high level of proactivity, commitment and energy
• Ability to work independently
• Excellent relationship builder
• Excellent problem solving skills
• Strong individual initiative, organizational skills, and multi-tasking abilities
• A flexible and “can do” attitude

Remuneration & other details

Remuneration & other details

- Excellent opportunity to be part of an innovative and top Biopharma company
- Full-time permanent employment (with DOCS, insourced 100% with our client)
- Office based in Solna
- Competitive salary level and great benefits

Apply for this job: Clinical Study Manager

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Marlow
Buckinghamshire
SL7 1HZ
England
Website:  Visit Our Web Site

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