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Associate Director, Clinical Project Scientist - Metabolism-6339131129
Description
Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for an Associate Director, Clinical Project Scientist - Metabolism, located in Raritan, NJ.
Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, oncology, infectious disease, diabetes, hematology, metabolic disorders, and immunologic disorders.
The Clinical Project Scientist position for Metabolism will be filled by a high performing individual who demonstrates a strong scientific and technical background, the highest personal and ethical standards and a track record for accomplishment in a team setting. Team matrix interactions may include project planning, regulatory affairs, data management, biostatistics, clinical pharmacology, global medical safety and other scientific and business related disciplines.
Responsibilities will include supporting/driving study design, development of essential documents such as protocols and protocol amendments, case report forms and informed consent and overall execution of clinical studies. Maintains expertise and understanding of documentation needed for data collection and analysis, regulatory requirements, policies and process. This person may act as a liaison between company and clinical investigators, and may thus be required to develop credible relationships with opinion leaders, medical directors, and key stakeholders. In concert with medical personnel, the person in this role will also be responsible for data review and medical monitoring/reporting activities, will evaluate adverse events (pre and post-marketing) for relationship to treatment, and may support the interpretation, reporting of results, and preparation for worldwide health authority submissions.
The successful candidate may present research results at internal/external meetings and investigator meetings. This person may also be responsible for reviews of medical literature and related new technologies.
Qualifications
A minimum of a Bachelor's degree is required, and advanced degree (e.g., MS, RD, PhD or PharmD) is preferred. A minimum of at least 6 or more years of clinical research and development experience within the pharmaceutical industry (Pharma, CRO, Biotech, etc.) is required. Experience in Internal Medicine or Metabolism product development is desirable.. Experience with cross company alliances also preferred. Significant experience in managing/supervising clinical trials, clinical research programs is required. Strong interpersonal and communication skills are essential. Must demonstrate ability to operate in a matrix environment. Ability to travel 5-10%.
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W: LI NA
Primary Location:North America-United States-New Jersey-Raritan
Organization: Janssen Research & Development, LLC. (6084)
Job: Clinical Research non-MD
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.
Associate Director, Clinical Project Scientist - Metabolism-6339131129
Description
Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for an Associate Director, Clinical Project Scientist - Metabolism, located in Raritan, NJ.
Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, oncology, infectious disease, diabetes, hematology, metabolic disorders, and immunologic disorders.
The Clinical Project Scientist position for Metabolism will be filled by a high performing individual who demonstrates a strong scientific and technical background, the highest personal and ethical standards and a track record for accomplishment in a team setting. Team matrix interactions may include project planning, regulatory affairs, data management, biostatistics, clinical pharmacology, global medical safety and other scientific and business related disciplines.
Responsibilities will include supporting/driving study design, development of essential documents such as protocols and protocol amendments, case report forms and informed consent and overall execution of clinical studies. Maintains expertise and understanding of documentation needed for data collection and analysis, regulatory requirements, policies and process. This person may act as a liaison between company and clinical investigators, and may thus be required to develop credible relationships with opinion leaders, medical directors, and key stakeholders. In concert with medical personnel, the person in this role will also be responsible for data review and medical monitoring/reporting activities, will evaluate adverse events (pre and post-marketing) for relationship to treatment, and may support the interpretation, reporting of results, and preparation for worldwide health authority submissions.
The successful candidate may present research results at internal/external meetings and investigator meetings. This person may also be responsible for reviews of medical literature and related new technologies.
Qualifications
A minimum of a Bachelor's degree is required, and advanced degree (e.g., MS, RD, PhD or PharmD) is preferred. A minimum of at least 6 or more years of clinical research and development experience within the pharmaceutical industry (Pharma, CRO, Biotech, etc.) is required. Experience in Internal Medicine or Metabolism product development is desirable.. Experience with cross company alliances also preferred. Significant experience in managing/supervising clinical trials, clinical research programs is required. Strong interpersonal and communication skills are essential. Must demonstrate ability to operate in a matrix environment. Ability to travel 5-10%.
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W: LI NA
Primary Location:North America-United States-New Jersey-Raritan
Organization: Janssen Research & Development, LLC. (6084)
Job: Clinical Research non-MD
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.