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Clinical Project Physician
View: 219
Update day: 20-03-2024
Location: Allschwil Basel-Landschaft BL
Category: Health / Medical Care
Industry: Medical Devices Biotechnology Pharmaceuticals
Position: Associate
Job type: Full-time
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Job content
- Salary: 110 - 120 CHF ph all-in
- REF Number: 00051740
- Consultant: Adrien Guimard
- Contact: 0041 (0) 800 106 106
- Date Published: 24.09.2021
- Sector: Basel Area
- Location: Allschwil, Manager
- Discipline: Clinical - Clinical Development
Main Responsibilities
- Responsible for medical monitoring/reporting and company safety officer activities
- Works on clinical development plans, trial protocols and takes ownership of clinical study reports
- Evaluates adverse events (pre and post-marketing) for relationship to treatment
- Assists Regulatory Affairs in determining requirements for any corrective actions or health authority reporting
- May act as a medical contact at the company for health authorities concerning clinical/medical issues
- Interprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions
- Close interactions with Project Scientists and Physicians across programs
- Assists Regulatory Affairs in the development of drug regulatory strategies
- Helps explore and evaluate new product ideas to assist in identifying new market opportunities
- Support general Clinical/Medical Affairs activitiesinvolving product evaluation, labelling and surveillance
- Participate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc.
- Reviews medical literature and related new technologies
- May be asked to assess medical publications emerging from the Team and its affiliates
- May be responsible, with appropriate colleagues, for review of Company advertising and promotional materials
- MD (or equivalent) in relevant area with appropriate post-doctoral training and certification
- Ideally previous experience in the Pulmonary Hypertension Therapeutic Area, otherwise Cardiovascular/Cardiopulmonary experience is appreciated.
- Experience in medical review.
- Submission experience a strong advantage.
- Fluent in written and spoken English
- Working knowledge of the use of Microsoft suite of software products including Excel and Word
- Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings
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Deadline: 04-05-2024
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