Study Responsible Physician
Johnson & Johnson
Allschwil, Switzerland
vor 6 Tg.

Caring for the world one person at a time inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people.

Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable

As part of the Janssen Pharmaceutical Companies of Johnson & Johnson in our Neuroscience TA, we are working to create a world without disease.

Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science.

We collaborate with the world for the health of everyone in it.

Janssen Pharmaceutical Companies of Johnson & Johnson, are recruiting for a

Clinical Project Physician

The Project Physician is a responsible member of a clinical team dedicated to the development and execution of medical strategies and the clinical and operational implementation of a complex compound program.

The Project Physician provides active medical and scientific contribution to a cross-functional clinical team. The Project Physician provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes ownership for the content of clinical study reports and relevant documents for regulatory filings.

Team matrix interactions include project management, finance, legal, quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management, medical writing, biostatistics, global medical affairs, clinical pharmacology, clinical operations, health economics, epidemiology and other scientific and business related disciplines.

The Project Physician may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area.

ESSENTIAL FUNCTIONS :

  • 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 activities involving product evaluation, labeling 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.
  • 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 activities involving product evaluation, labeling 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.
  • OTHER RESPONSIBILITIES / DETAILED DUTIES :

    Education :

    MD (or equivalent) in relevantarea with appropriate post-doctoral training and certification

    Required Technical Knowledge andSkills :

  • Fluent in written and spoken English
  • Working knowledge of the use of Microsoft suite of software productsincluding Excel and Word
  • Experience and knowledge of Good Clinical Practices and regulatoryrequirements for the conduct of clinical trials and for the appropriatecontributions to regulatory filings
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