Director of Clinical Development

  • Proclinical
  • Switzerland
  • 19/08/2020
Full time Data Science Data Analytics Big Data Data Management Statistics

Job Description

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.