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Job Details

Associate Director Of Clinical PM

Company: CK Clinical
Location: Zürich
Reference: CL40669
Closing Date: 20 Dec 17
Type: Contract
Salary (£): Negotiable
Benefits:

Job Summary:

Jocelyn Blackham is currently recruiting for an Associate Director of Clinical Project Management to join an innovative target based drug discovery team for an international...

Requirements:

Jocelyn Blackham is currently recruiting for an Associate Director of Clinical Project Management to join an innovative target based drug discovery team for an international pharmaceutical company based in Zurich, Switzerland. This role is offered on a full time temporary basis for 12 months, with the possibility of extension.

Your main objectives in this role will be to:
• Hold responsibility for the oversight, conduct, and ongoing management of vendors for assigned complex clinical trials
• Provide oversight of clinical studies in compliance with procedural documents, SOPs, Code of Federal Regulations, Good Clinical Practices, ICH Guidelines, and all applicable regulations within the Clinical Development Plan (CDP) and according to the VBU operating model
• Provide leadership of the cross functional Study Execution Team (SET), to ensure study objectives and KPIs are met with expected quality, on schedule and on budget
• Hold responsibility for continuous monitoring of KPIs and Metrics compliance, study specific risks and mitigation solutions, timelines & budget for assigned studies
• Provide study level updates and summaries to the Program Operational Oversight Lead (POOL) ensuring that any study issues, with proposed solutions, are escalated as appropriate
• Assist in the management of the study budget, including Task Orders, Change Orders, invoice approval and financial reconciliation process.
• Take responsibility for the roll-out and maintenance in assigned clinical studies of risk-management approach defined for program
• Manage vendors working on assigned study, including setting expectations, training, managing timelines and deliverables, and issue management

You are required to have the following qualifications, skills and experience:
• B.S. degree in related discipline, preferably in life science, or equivalent. Advanced degree is highly desirable
• Previous experience in clinical study/program management role in the pharmaceutical industry including CRO experience.
• Vaccine clinical study/program management would be beneficial
• Strong leadership is essential - previous line management /matrix management/ team experience would be advantageous
• Strong expertise in clinical study delivery and oversight
• Knowledge of local and international regulations and guidelines
• Experience in successful change management (strategy, initiation, development and implementation of important, organization wide changes) is desirable

If you are employed by this client you will be joining an international pharmaceutical company based in Zurich. 

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL40669 in all correspondence.

Apply for this job: Associate Director Of Clinical PM

Contact Information:

Address:  Head Office
9 High Street
Stevenage
Hertfordshire
SG1 3BG
England
Tel:  +44 (0)1438 743047
Fax:  +44 (0) 1438723800
Website:  Visit Our Web Site

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