Director of Clinical Development job in Switzerland

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First Name*

Last Name*

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Phone Number*

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Are you an employer or a jobseeker?*

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First Name*

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Job type: Permanent

Discipline: VP/Head of Clinical Operations

Location: Switzerland

This vacancy has now expired. Please see similar roles below...

Due to its expanding portfolio, a large biopharmaceutical company has an excellent opportunity for a Clinical Development Director for our cardiorenal therapy area. This role will be a part of our global clinical development team based in Switzerland.

Job Responsibilities

Leadership of clinical study/program to ensure delivery of clinical trials per ICH-GCP requirements and meeting timelines and budget
Leadership and moderation of clinical advisory boards and ongoing interactions with applicable committees relevant to successful conduct of studies and programs
In collaboration with a cross-functional team, drive the development of effective and innovative clinical trial designs, and facilitate execution of clinical trials by supporting site and CRO personnel, safety monitoring activities, data clean-up activities, data analyses, and clinical study report development and finalization
Author protocols, and provide scientific input into manuscripts/publications, IBs, regulatory and study reports
Research and analyse scientific/medical information and data with respect to clinical trials, safety databases, and other medical/scientific elements necessary for decision-making and regulatory submissions
Assess safety data including labs and SAEs on an ongoing basis for ongoing clinical trials; manage DSMB processes for clinical trials
Represent the company as the scientific subject matter expert at external meetings including those with Investigators, Steering Committees, Key Opinion Leaders and Advisory Groups
Provide Medical Oversight and Medical Monitoring to interventional clinical trials (supported by CROs, if applicable)
Maintain and evaluate current knowledge of key disease areas, providing information to appropriate groups as needed
Evaluate investigator-initiated protocols and make recommendations (if applicable)

Skills and Requirements:

MD (strongly preferred) or internationally recognized equivalent degree or PhD in science/health-related discipline
6 to 8 years of pharmaceutical industry experience gained in clinical research
Experience in phase 3 and 4 clinical studies/outcomes trials is an advantage
Knowledge and experience of clinical trial design, data analysis, statistics and research methods
Knowledge of the drug development process and clinical research methodologies
Trained in GCP regulations, and familiar with ICH and FDA guidelines relevant to clinical development
Ability to work independently and in a fast paced, hands-on, flexible, dynamically changing environment

To Apply

In case you have difficulty in applying or if you have any questions, please contact Tom Russell on +44 203 8246 104 or upload your CV on our website - www.proclinical.com/send-cv

A full job description is available on request.

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