Johnson & Johnson Careers

Clinical Project Physician

Cherry Hill, New Jersey; Allschwil, Switzerland
Clinical Research MD

Job Description

Requisition ID: 2764190425

Actelion Pharmaceuticals Ltd., a Janssen Pharmaceutical Company of Johnson & Johnson, is recruiting for an office-based Clinical Project Physician located in Cherry Hill, New Jersey, USA, or in Allschwil, Switzerland.
At 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 are Janssen. We collaborate with the world for the health of everyone in it. Learn more at and follow us @JanssenGlobal. Actelion Pharmaceuticals Ltd. is part of the Janssen Pharmaceutical Companies.
Actelion is a leader in the field of pulmonary hypertension and specializes in rare cardiopulmonary diseases. Our portfolio of pulmonary arterial hypertension (PAH) treatments covers the spectrum of disease, from World Health Organization (WHO) Functional Class (FC) II through FC IV, with oral, inhaled and intravenous medications.
In this exciting position you will perform the following:
  • Provide medical support internally for all Clinical Development Science (CDS) - responsible project activities through a comprehensive understanding of the science, medicine, product environment and competitive landscape relating to the disease area
  • Provide medical support externally based on thorough scientific review of relevant product data and consultation with internal and external experts
  • Be the key physician contact for sites and investigators during study start-up and study execution, act as a liaison between the company and clinical investigators, CRO’s, and CRA’s
  • Present trial- and compound- related information at Investigator Meetings and internal training sessions
  • Participate in medical review, interpretation, and reporting of the results of the research, including submission to health authorities
  • Prepare medical narratives on research subjects as needed
  • Maintain knowledge of therapeutic area(s) and indications, as well as maintaining of relevant regulations and guidelines to ensure safe and ethical conduct of trials
  • Attend relevant medical conferences and therapeutic area training as needed and maintain knowledge of key publications
  • Support the assessment of new in-licensing opportunities and business development activities / due diligence evaluations
Provide medical leadership internally:
  • Contribute medical and scientific input
  • Obtaining complete understanding of all clinical data for assigned compound
  • Undertake product and therapeutic area reviews and provide evidence-based input to the study-related, strategic and regulatory documents
  • Support delivering the medical aspects of the Clinical Project Development Plan (CDP) related to the indication and executing its implementation
  • Contribute to the core medical/scientific information required in all clinical documents (e.g., protocols, statistical analysis plans, core informed consent forms, clinical study reports, investigators’ brochure, clinical components of regulatory submissions, safety related documents), and assure production of high-quality documents
  • Provide medical input on behalf of CDS to the monitoring and analysis of the safety profile of the product together with Global Drug Safety
  • Responsible for ensuring projects are adequately supported medically and prioritized to ensure timely and on-target delivery on set objectives and deliverables in line with clinical development goals
  • Interface medically with affiliates as needed to provide product and therapeutic area training and to raise global project awareness for the product, both to stimulate recruitment and prepare the ground for potential future commercialization
Provide external medical leadership:
  • Support the development and maintenance of contacts with Key Opinion Leaders and Investigators
  • Support the organization of and active participation in the medical aspects of clinical advisory boards, investigator meetings, steering committee meetings, adjudication committee meetings, partners meetings, and data monitoring committees
  • Contribute to clinical/scientific content for submissions to regulatory agencies and IRBs / ethics boards, and answer to medical/scientific questions from Health Authorities
  • Execute publication and clinical communication strategy in coordination with Medical Communications

  • MD with at least 5 years of clinical / research experience
  • Sound knowledge of drug development and clinical trial process
  • Strong knowledge of regulatory requirements / International Council of Harmonzation (ICH) guidelines
  • Good organizational skills, and able to effectively work as part of a team in a matrix environment and independently
  • Motivated and energetic individual with high personal and ethical standards
  • Flexible mindset, agile, and able to deliver on timelines and strict deadlines
  • Demonstrated ability to think strategically
  • Excellent communication skills.  Strong verbal, written, and presentation skills are essential
  • Detail-oriented with a hands-on approach
  • If based in the Cherry Hill (New Jersey) office, then international travel to the headquarters required, for at least 20% of the time
  • Other intermittent domestic and international travel as well (not expected to be more than 10%-15% of the time on average)
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location
United States-New Jersey-Cherry Hill-
Other Locations
Europe/Middle East/Africa-Switzerland-Allschwil
Janssen Research & Development, LLC. (6084)
Job Function
Clinical Research MD
Requisition ID