Job Detail

Global Medical Information Manager180000FX 

Actelion Pharmaceuticals, a Janssen Pharmaceutical Company of Johnson & Johnson, is recruiting for an expert-level (Associate Director),  Global Medical Information Manager in  Allschwil .

 

As part of the Janssen Pharmaceutical Companies of Johnson & Johnson, 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.

 

Actelion is a leader in the field of pulmonary hypertension (PH). Our portfolio of PH treatments covers the spectrum of disease, from WHO Functional Class (FC) II through to FC IV, with oral, inhaled and intravenous medications.

  
Role Responsibilities

• Develop responses for simple and complex medical inquiries: formulation of the strategy and framework within which a response lies


• Conduct comprehensive literature searches in relation with a medical inquiry. Identify and weigh the information available


• Prepare, finalize and update global standard response documents, based on knowledge of clinical studies, therapeutic areas, and new information appearing in the literature


• Communicate with internal reviewers to finalize document


• Compile and maintain comprehensive, accurate and up-to-date competitor compendiums to provide Clinical Development with scientific and clinical insights on products and treatment trends for Actelion new disease areas


• Provide an information support service to the clinical and marketing teams. Includes the distribution among other departments of data relating to medical information inquiries and GRDs as well as ad hoc/bespoke activities relating to medical information that support the broader needs of the organization


• Propose process improvements to enhance the global medical information service from a methodology, process and compliance perspective


• Manage and track inquiries with standard medical information databases


• Transmit any reported adverse events to Global Drug Safety in a timely manner


• Develop and maintain good relationships with internal departments and external contacts

 
Candidate Requirements

• Ph.D or PharmD level degree, with thorough grounding in clinical pharmacotherapy


• 5+ years pharmaceutical industry experience in medical information, medical communication or regulatory affairs


• Demonstrated scientific/medical writing experience


• Must have a broad knowledge and understanding of products and diseases that allows for the provision of complex information that is accurate and meets all regulatory requirements


• Knowledge of relevant information sources including: printed publications, unpublished sources, databases, websites, company departments, external bodies


• Ability to analyse and appraise clinical, biomedical and scientific reports in a systematic, fair and balanced way


• Can understand and apply principles, concepts and standards


• Ability to work with ambiguity and complex situations


• Excellent organizer and communicator


• Ability to work independently and as part of a team


• Fluent in written and spoken English

If you are interested in making an impact by working in a culture of innovation, trust and teamwork, we welcome your application. 

Primary Location

: CH-BL-Allschwil

Schedule

: Full-time

Job Posting

: Oct 24, 2018

Job Type

: Standard

Job

: Clinical Development