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Associate Medical Director Hematologic Malignancies, US Medical Affairs Job (Horsham, PA, US)

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Associate Medical Director Hematologic Malignancies, US Medical Affairs-0607141124

Description

Janssen Biotech, Inc., a member of the Johnson & Johnson Family of Companies, is recruiting for an Associate Medical Director for Hematologic Malignancies, US Medical Affairs, located in Horsham, PA. The Hematologic Malignancies group, which is an integral part of the Medical Affairs Medical Group, provides Medical Affairs support for drugs such as ibrutinib (Imbruvica), daratumumab, and siltuximab (Sylvant), as well as products under development.

For more than 30 years, Janssen Biotech, Inc. has delivered on the promise of new treatments and ways to improve the health of individuals with serious disease. Built upon a rich legacy of innovative firsts, Janssen pursues innovative solutions in diverse therapeutic areas including oncology (solid tumors and hematologic malignancies), immunology, urology and nephrology. Janssen is dedicated to delivering solutions for the unmet needs in these disease states. Rich scientific collaborations and community-based relationships provide us access to some of the top minds in science today, allowing us to advance the treatment of patients through our innovative medicines. Our discoveries lead us not only to new treatments, but also to new ways to empower patients and expand their access to quality care.

Janssen thrives on a diverse company culture, celebrates the uniqueness of our employees, is committed to inclusion, and is proud to be an equal opportunity employer.

The Associate Medical Director for Hematologic Malignancies, US Medical Affairs, will have multiple responsibilities: 1) Provision of strategic support as a therapeutic area expert to multiple internal groups within JBI (Marketing, Sales Training, Research & Development, Business Development, Medical Communications, Medical Writing, Global Medical Safety, and the Clinical Science Liaison Team); 2) Responsibility for the development and execution of Medical Affairs sponsored and supported clinical programs (i.e. study design, protocol development, execution, and supervision of Medical Affairs clinical studies of all types) including development and execution of Phase IIIb and IV clinical trials, and assessment of Investigator Initiated Clinical Research applications; 3) Provision of peer-to-peer responses to unsolicited medical information queries from practicing hematologists, oncologists and other health care providers; 4) Coordination of efforts within Medical Affairs to address medical and scientific issues and provide scientific and clinical support to ensure the appropriate use of all Janssen marketed products for hematologic malignancies; 5) Support of the Oncology business in the development of compliant promotional materials and the training of product representatives; 6) Collaboration with R&D teams in the evaluation of new molecules for the treatment of oncologic disease; 7) Relationships with external investigators and opinion leaders through participation in Advisory Boards, national and international society meetings, and other venues; 8) Support of the development of scholarly publications arising from Janssen Biotech studies; 9) Support of the mission of Medical Affairs in developing product monographs and responding to unsolicited written and verbal product inquiries and surveillance of product safety; and 10) Other duties and responsibilities within the group as requested by its leadership.

This individual will play an important role in the development and review of scientific publications, investigation of safety issues, and assessment of licensing and acquisition opportunities. This individual will work closely with the Regulatory Affairs, Pharmacovigilance, and Marketing and Sales Groups.

Qualifications


This position requires an MD with training in Oncology and/or Hematology. Board certification or eligibility Medical Oncology or Hematology is required. Clinical trial experience (i.e. trial design, protocol writing, etc.), especially experience in investigational drug study design and conduct (Phases II-IV) within the pharmaceutical industry, CRO or academia; is highly preferred. Excellent written, oral and presentation skills and strong organizational skills are required. A demonstrated ability to work in a matrix type environment with interaction with cross-functional teams is preferred. This position requires up to 25% annual travel (domestic and international).

BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.

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Primary Location:North America-United States-Pennsylvania-Horsham
Organization: Janssen Scientific Affairs, LLC (6120)
Job Function: Medical Affairs

Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.

Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.

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