Senior Clinical Director, Hematology

This is a fully remote position, open to applicants in New Jersey, +1 more state.

📋 Description

• Plan and oversee clinical research operations related to both new and existing medicines in the field of Hematology.

• Manage the entire clinical development cycle, which includes study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.

• Assess pre-clinical and translational research to develop early clinical development plans and Investigational New Drug applications.

• Formulate clinical development strategies for investigational or marketed Hematology pharmaceuticals.

• Organize clinical trials and collaborate on operational strategies.

• Provide medical oversight and ensure the proper conduct of clinical trials.

• Analyze and summarize clinical findings to support safety, efficacy, applications, clinical study reports, and publications.

• Participate in both internal and joint internal/external research project teams.

• Assist in business development evaluations of external opportunities.

• Collaborate with various functional areas to facilitate study execution.

• Work alongside commercialization, regulatory affairs, statistics, and manufacturing specialists.

• Update leadership and relevant personnel regarding study progress and competitor products.

• Provide expert scientific insights both internally and externally.

• Maintain scientific knowledge and stay informed about advancements in Hematology and related disciplines.

• Identify and engage with clinical investigators.

• Attend scientific conferences and meetings.

• Draft development documents, presentations, budgets, and position papers.

• Foster collaborations with external researchers globally.

• Travel for company business to oversee clinical research projects.

⛳️ Requirements

• M.D. or M.D./Ph.D. degree.

• Experience in the industry or as a senior faculty member in academia.

• At least 3 years of clinical medicine experience.

• A minimum of 3 years of industry experience in drug development or biomedical research experience in academia.

• Proven success in supervising clinical studies and protocols.

• Established record of scientific scholarship and accomplishment.

• Demonstrated expertise in clinical medicine and a background in biomedical research.

• Strong interpersonal skills and the ability to work effectively in a team setting.

• Exceptional verbal and written communication and presentation abilities.

• Required skills include: Clinical Development, Clinical Medicine, Clinical Pathways, Clinical Research Management, Clinical Trial Development, Data Analysis, Ethical Standards, Hematology, Intellectual Curiosity, Oncology, Pathology, Regulatory Affairs Compliance, Regulatory Reporting, Scientific Consulting, and Strategic Planning.

• Candidates must be residents of the US or Puerto Rico only.

• Visa sponsorship is not available.

• Must be open to approximately 25% travel.

🏝️ Benefits

• Annual bonus.

• Long-term incentive, if applicable.

• Comprehensive medical, dental, and vision healthcare plans.

• Additional insurance benefits for employees and their families.

• Retirement benefits, including a 401(k) plan.

• Paid holidays.

• Vacation time.

• Compassionate leave.

• Sick leave.

• Option for remote work arrangements.