Associate Medical Director, Clinical Sciences, Oncology (Solid Tumors)

Tarrytown, NY, United States
Oct 30, 2020
Required Education
Position Type
Full time
The Associate Medical Director crafts clinical study concepts which lead to clinical trial protocols with responsibility to supervise individual clinical trials. Working closely with supervisor, contributes to the Clinical Development Plan (CDP) that meets international regulatory standards.A typical day might include the following:
  • Defines clinical trial-related goals and objectives.
  • Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSCs) based on thorough scientific review and consultation with specialists.
  • Reviews and finalizes the medical and scientific portions of clinical trial protocols and amendments.
  • Reviews and edits documents related to trials, such as monitoring plans, SAPs, amendments, IRB submissions and regulatory submissions.
  • Leads and supervises the Clinical Team to produce high quality program results on schedule
  • Identifies program, trial or data risks, crafts and implements mitigation strategies
  • Maintains and develops relationship with study investigators
  • Reports to supervisor and management on clinical trial findings and breakthroughs
  • Analyzes the benefits and risk aspects of an assigned therapeutic candidate
  • Analyzes clinical data and monitors safety
  • Responsible for activities and procedures that ensure patient safety
  • Ensures Clinical Team compliance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety
  • Is the primary clinical contact for communications with regulatory agencies and IRBs/ethics boards
This role might be for you if:
  • You want to make a broader impact by developing new, innovative therapies for patients with serious diseases
  • You have outstanding work ethis with focus on details and high quality results
  • You work effectively in a matrixed environment and collaborate well within teams and with CROs
  • You build successful collaborations with internal and external partners
  • You are able to develop original ideas
  • You have superior written and verbal communication and presentation skills
For this position we seek an MD or MD/PhD with Oncology or relevant clinical training. Clinical research and/or basic science research experience in an academic setting preferred.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.