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;
Requirements
Qualifications
- 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
Benefits
- 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.

Join the Brunel Family
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Sending an application is quick and easy. Just make sure you have the required documents ready to go.
- Certifications (optional)
- Job references (optional)
- Motivation Letter (optional)
- Resume or up-to-date LinkedIn / Xing profile
Any questions remaining?
Your consultant, Diana Grodowski is happy to clarify anything about this vacancy. When reaching out, use the pub number:
PUB291854
Account manager
Diana Grodowski
Brunel Canada - Toronto
d.grodowski@brunel.net
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