Senior Clinical Research Director - Oncology
Scorpion Therapeutics, Convent Station, New Jersey, us, 07961
Role Summary
Senior Clinical Research Director - Oncology role focused on leading the clinical trial strategy for multiple myeloma assets. You will coordinate with Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish and execute development plans. Location: Cambridge, MA; Morristown, NJ with potential travel to Vitry, France; travel may be required. Responsibilities
Working within a matrix model, establish or adapt clinical development and contingency plans by engaging with clinical investigators, advisors and regulatory authorities. Author protocols, extended synopses, clinical sections of the Investigator Brochure, IND/IMPD fillings, annual reports, development risk management plans. Lead the clinical interpretation of study results. Contributes to clinical study reports and clinical summaries, including regulatory submissions. Provide expert medical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine, to ensure optimal planning and execution of clinical trials. Present and discuss development strategy and clinical study results with key internal stakeholders, external investigators, advisory boards, and regulatory authorities. Author clinical abstracts, presentations for conferences, and manuscripts. Qualifications
Required: At least 4 years experience in clinical development in the pharmaceutical industry, CRO, or healthcare institution. Preferred: Experience in myeloma or hematologic malignancies. Skills
Excellent communication skills (verbal and written English) with both internal and external stakeholders Adept at problem solving Thoughtful risk-taking: challenge decisions and status quo with a risk-management approach Demonstrated ability to work with a multi-functional team to achieve project milestones Understanding of and willingness to meet applicable regulatory, quality and compliance standards Quality-focused, adept at developing good practices, open-minded to data-driven approaches and new digital solutions International/intercultural working skills Education
Medical Doctor (MD) or equivalent; training in Oncology and/or Hematology, preferably with experience in myeloma or hematologic malignancies is a plus.
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Senior Clinical Research Director - Oncology role focused on leading the clinical trial strategy for multiple myeloma assets. You will coordinate with Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish and execute development plans. Location: Cambridge, MA; Morristown, NJ with potential travel to Vitry, France; travel may be required. Responsibilities
Working within a matrix model, establish or adapt clinical development and contingency plans by engaging with clinical investigators, advisors and regulatory authorities. Author protocols, extended synopses, clinical sections of the Investigator Brochure, IND/IMPD fillings, annual reports, development risk management plans. Lead the clinical interpretation of study results. Contributes to clinical study reports and clinical summaries, including regulatory submissions. Provide expert medical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine, to ensure optimal planning and execution of clinical trials. Present and discuss development strategy and clinical study results with key internal stakeholders, external investigators, advisory boards, and regulatory authorities. Author clinical abstracts, presentations for conferences, and manuscripts. Qualifications
Required: At least 4 years experience in clinical development in the pharmaceutical industry, CRO, or healthcare institution. Preferred: Experience in myeloma or hematologic malignancies. Skills
Excellent communication skills (verbal and written English) with both internal and external stakeholders Adept at problem solving Thoughtful risk-taking: challenge decisions and status quo with a risk-management approach Demonstrated ability to work with a multi-functional team to achieve project milestones Understanding of and willingness to meet applicable regulatory, quality and compliance standards Quality-focused, adept at developing good practices, open-minded to data-driven approaches and new digital solutions International/intercultural working skills Education
Medical Doctor (MD) or equivalent; training in Oncology and/or Hematology, preferably with experience in myeloma or hematologic malignancies is a plus.
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