Clinical Program Director

Hobson Prior currently have an exciting opportunity for a Clinical Program Director to join a Global Clinical Development Department at a top pharmaceutical company on permanent basis in either Monheim (Germany), Brussels (Belgium), Slough (UK) or Raleigh (US).

Job Responsibilities:

• This position will be responsible for all clinical aspects of their assigned programs/missions.
• Lead and ensure adequate planning, design, defense, and implementation of the clinical development strategy including generation and appropriate revision of the Clinical Development Plan, clinical aspects of the Target Patient Value Profile, and the Investigators Brochure.
• You will provide leadership of the relevant clinical programs Phase 2 - 4.
• Developing a strong knowledge base of the relevant disease area and therapeutics and becoming the company expert for the respective treatment modality.
• You will lead or contribute to the development and subsequent revisions of the CDP ensuring compatibility with the TPVP and representing contemporary research approaches.
• Ensuring that study concepts and final protocols related to the relevant clinical development plans are of high quality, represent contemporary research approaches, are aligned with related CDPs and TPVPs, and are appropriately managed by the clinical study teams.
• Developing and maintaining excellent working relationships and global cross functional collaboration together with all necessary stakeholders to ensure broad medical, scientific, regulatory, commercial and external input into the clinical programs.

Key Skills:

• Demonstrates clear and articulate verbal, written and presentation skills with excellent command of the English language.
• Project management skills preferred.
• A participative management style.
• Ability to build effective team relationships with colleagues at all levels in the organization.
• Ability to work in a matrix type environment.

Requirements:

• Master's Degree is required with a PharmD, PhD or MD preferred.
• A minimum of 3 to 5 years of relevant experience in biopharmaceutical clinical development is required, including the management of multiple clinical studies.
• Knowledge of clinical study designs that apply real world evidence (integrated patient databases such as claims and EMR) to clinical care is helpful.
• Demonstrated ability to think creatively and develop solutions using retrospective study designs with consideration of real-world evidence a plus
• Experience supporting the development of submissions and presenting to regulatory authorities (e.g., FDA, EMA, PMDA).
• Experience in development and execution of paediatric plans preferred.
• Knowledge of relevant therapeutic area (neurology) with epilepsy experience preferred.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.