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Global Clinical Development Director
View: 133
Update day: 25-04-2024
Category: R & D IT - Software
Industry: Medical Equipment Manufacturing Biotechnology Research Pharmaceutical Manufacturing
Position: Director
Job type: Full-time
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Job content
Proclinical are recruiting a Global Clinical Development Director for a pharmaceutical corporation. This role is on a permanent basis and is located in Zug with hybrid working available. The client is focused on ground-breaking in neuroscience.Responsibilities
- Serve as a medical SME for internal resources.
- Guarantee compliance with GCP, ethical, scientific, and medical regulations, and statutory principles during all clinical development actions.
- Offer clinical and medical contributions for all clinical deliverables in the affiliated program.
- Provide input to medical supervising to guarantee data integrity and coherence of data comprehension under the direction of target product profile and clinical development plan.
- You will operate on multifaceted matters where analysis of situations or data needs exhaustive knowledge of the therapeutic area.
- To complete clinical team objectives and implementation of the clinical programs, you will make final decisions on clinical and medical matters, assisting clinical operations.
- Assist the project team in all medical, scientific, and clinical matters throughout study performance.
- Other duties may be assigned to this role.
- Educated to a MD degree level in a pertinent discipline.
- At least 10+ years of experience in a pharmaceutical or biosimilar role.
- At least 5+ years of experience in senior functions with a decision-making authority.
- Ability to guide clinical development.
- Experience in immunology clinical or drug development.
- Familiarity with assisting in archiving and regulatory proposals.
- Comprehension of GCP / stats background / registrational study designs.
- Acquaintance with biosimilars.
- Prior involvement in European and the US clinical development pathways.
- Conform to company SOPs, GCP, governmental policies, guidelines, statutory regulations and suitable laws regulating drug development and clinical research.
- Adopt efficient, positive engagements with the expert bodies of multiple nature and corporate associates.
- Familiarity with comprehension of clinical needs, guidelines, regulations, policy statements, etc.
- Capable of guiding and influencing project teams, committees, etc., to obtain group objectives.
- Leadership abilities.
- Communication skills both verbally and in writing.
- Able to represent the division in senior internal forums, committees and external meetings.
- Interpersonal capabilities.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#MedicalAffairs
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Deadline: 09-06-2024
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