Senior Clinical Development Director


About this role

  • We’re hiring a Senior Director of Clinical Development for our client, a clinical Oncology company located in Boston Massachusetts;
  • This role is open to residents located within the US that are willing to relocate to Boston Massachusetts

  • The Senior Director, Clinical Development coordinates with the other members of the research team, which includes representatives from clinical operations and the researchers;
  • He or she is responsible to liaise with the company management team, various vendors, and study investigators at participating sites;
    Duties and Responsibilities
  • Assist in building a team of clinical scientists based on expanding program needs;
  • Provide mentoring to and leadership for junior clinical scientists;
  • Review of clinical and scientific data and developing product knowledge to understand and communicate the relevant information;
  • Developing and reviewing study protocols and protocol amendments;
  • Contribute relevant clinical sections to documents such as the IB, DSUR or INDs;
  • Responsible for drafting reports, abstracts, posters, CSRs and presentations on the various findings of the clinical research;
  • Providing senior management personnel regular updates on the progress of the clinical research;
  • Lead dose escalation calls for phase 1 studies and/or safety review meetings;
Perform regular review of clinical data to ensure safety procedures are followed, efficiency is maintained, and lab data are accurate and correct



  • Bachelor of Science degree from an accredited educational institution;
  • Additional training in bio life sciences with an advanced master's qualifications is preferred;
  • Training through internships that provide knowledge on ICH, GCP, and other relevant regulatory guidelines is advantageous;
  • At least 10 years previous experience in large pharma and/or biotech sectors;
  • Prior experience either mentoring or managing other clinical scientists is required;
  • Ability to write clinical protocols;
  • Ability to perform relevant literature reviews, succinctly summarize results from the literature review and apply results to the program;
  • Analytical capabilities;
  • An eye for details;
  • Time management skills;
  • Strong communication and interpersonal abilities;
  • Ability to interact with scientists (both internal and external), clinical investigators and other medical experts;
  • Capable to read and understand clinical information;
  • Willing to travel


  • Why work through Brunel? We
    start with competitive rates, a comprehensive benefits package and a safe
    on-boarding process;
  • With our industry insights and recruiter expertise, we are
    supporting projects and clients worldwide;
  • With Brunel you gain experience and
    expertise, building on your skills and developing your career further.
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Any questions remaining?

Your consultant, Diana Grodowski is happy to clarify anything about this vacancy. When reaching out, use the pub number:

Account manager

Diana Grodowski
Brunel Canada - Toronto

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