Senior Director/Director, Clinical Research Physician - Oncology
Janssen Research & Development, L.L.C, a member of the Johnson & Johnson Family of Companies, is recruiting for a Director/Sr. Director, Clinical Rseearch Physician for Early Development Oncology. The preferredlocation for this position is Spring House, PA, but consideration could be given to other locations. Up to 25% travel may be required. Remote work options may be considered on a case-by-case basis and if approved by the Company. The Oncology Therapeutic Area is seeking a physician-scientist to serve as a Senior Director/Director, Clinical Research working on novel anti-cancer compounds in early stages of development, from First-in-Human/Phase 1 until Proof of Concept. In this role, you will reside within the Experimental Medicine and Early Development group and report to the Early Development Clinical Leader for Hematologic Malignancies. You will be responsible for the development and execution of early stage clinical projects as a member of the cross-functional Compound Development Team and as the co-leader of the Clinical Study Team. The Senior Director/Director, Clinical Research will be responsible for the following:
-Design and conduct early clinical Phase 1 and Proof-Of-Concept development trials, assess clinical safety and efficacy data, and write clinical study reports, clinical sections of INDs, Investigator Brochures, etc. -You will also work closely with biomarker, discovery and translational research scientists. You will interpret reports, prepare oral and written results of product research, and participate in the discussion of strategies formulated within the Tumor Strongholds in disease areas such as prostate or lung cancer. This role requires:
-A high-performing physician-scientist familiar with clinical and translational research involving biomarkers and correlative laboratory clinical trial endpoints. -You will be required to collaborate closely with relevant functions within Janssen Pharmaceuticals including discovery, translational, and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists, as well as personnel from Global Clinical Operations, Global Strategic Marketing, and other support functions. -To be successful in this role, you will work closely with research group leaders, drug discovery teams, and project clinical teams. The ability to communicate effectively with basic laboratory scientists and clinical teams is critical. -You will be expected to establish strong working relationships and collaborations with external study investigators, key opinion leaders in drug development, and external alliance partners. Qualifications Qualifications - External -An M.D./Ph.D. or a MD with significant scientific research experience. -Formal training in Oncology or Hematology with Board certification or eligibility is preferred. -A minimum of 5
years' experience in clinical research within the pharmaceutical industry or academia is preferred. -Significant knowledge of translational and clinical cancer research and its application to cancer drug development is of paramount importance. -A working knowledge of the key areas of early drug development, including chemistry, biology, toxicology and early clinical development is required. -Knowledge of clinical pharmacology and its relationship to decision-making in early drug development is of value. -Alternatively you could have experience in clinical development, specifically experience in conducting phase II or III clinical trial and deep understanding of relevant regulatory health authority expectations and regulations. -Ability to strategize and lead a goal oriented clinical development team will be very valuable.
Salary Range:
$150K -- $200K
Minimum Qualification
Life SciencesEstimated Salary: $20 to $28 per hour based on qualifications.
-Design and conduct early clinical Phase 1 and Proof-Of-Concept development trials, assess clinical safety and efficacy data, and write clinical study reports, clinical sections of INDs, Investigator Brochures, etc. -You will also work closely with biomarker, discovery and translational research scientists. You will interpret reports, prepare oral and written results of product research, and participate in the discussion of strategies formulated within the Tumor Strongholds in disease areas such as prostate or lung cancer. This role requires:
-A high-performing physician-scientist familiar with clinical and translational research involving biomarkers and correlative laboratory clinical trial endpoints. -You will be required to collaborate closely with relevant functions within Janssen Pharmaceuticals including discovery, translational, and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists, as well as personnel from Global Clinical Operations, Global Strategic Marketing, and other support functions. -To be successful in this role, you will work closely with research group leaders, drug discovery teams, and project clinical teams. The ability to communicate effectively with basic laboratory scientists and clinical teams is critical. -You will be expected to establish strong working relationships and collaborations with external study investigators, key opinion leaders in drug development, and external alliance partners. Qualifications Qualifications - External -An M.D./Ph.D. or a MD with significant scientific research experience. -Formal training in Oncology or Hematology with Board certification or eligibility is preferred. -A minimum of 5
years' experience in clinical research within the pharmaceutical industry or academia is preferred. -Significant knowledge of translational and clinical cancer research and its application to cancer drug development is of paramount importance. -A working knowledge of the key areas of early drug development, including chemistry, biology, toxicology and early clinical development is required. -Knowledge of clinical pharmacology and its relationship to decision-making in early drug development is of value. -Alternatively you could have experience in clinical development, specifically experience in conducting phase II or III clinical trial and deep understanding of relevant regulatory health authority expectations and regulations. -Ability to strategize and lead a goal oriented clinical development team will be very valuable.
Salary Range:
$150K -- $200K
Minimum Qualification
Life SciencesEstimated Salary: $20 to $28 per hour based on qualifications.
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