Sr. Director, Clinical Operations

Sr. Director, Clinical Operations – Perm – Cambridge, MA. - $250,000 - $295,000
The end client is unable to sponsor or transfer visas for this position; all parties authorized to work in the US without sponsorship are encouraged to apply.

An American Company is seeking a Sr. Director, Clinical Operations in Cambridge, MA.

Role Description

The Director/Sr. Director, Clinical Operations Study Management serves as an expert in clinical
operations processes and is responsible for developing and sharing best practices within his/her team
and across the Clinical Operations organization. He/she will work with other Clinical Operations and
Expertise Area leaders to formulate strategies, standards, processes and best practices to be
implemented for the benefit across Clinical Operations.

The Director/Sr. Director, Clinical Operations Study Management ensures strong interaction with local
country, medical affairs teams/regional medical groups and other strategic partners as needed for the
successful delivery of clinical trials.

• Partners directly with or guides internal staff along with the CRO team(s) to collaborate with
preclinical (pharmacology, toxicology, drug safety and metabolism), regulatory affairs, medical
monitoring, biometrics, medical affairs, pharmacovigilance, and/or medical writing to develop drug
development strategies, protocol and study designs, and other key study and program deliverables. Has
overall accountability for the development of the Clinical Operations study/project strategy for assigned
projects.
• Communicates program strategy, goals and priorities across a wide range of audiences ensuring that
they are understood and supported.
• Active participation as a member of the Clinical Operations Leadership Team in driving strategy and
team execution.
• Participates in protocol, IB, ICF, Regulatory submission documents, CRF, CSR, abstract and publication
development and review and provides direction to junior staff to manage the content and process, as
necessary.
• Effectively discusses and presents study data across the company and with development partners;
collaborates with medical writers and investigators to write, present and/or publish data.

Why Hays?

You will be working with a professional recruiter who has intimate knowledge of the industry and market trends. Your Hays recruiter will lead you through a thorough screening process in order to understand your skills, experience, needs, and drivers. You will also get support on resume writing, interview tips, and career planning, so when there’s a position you really want, you’re fully prepared to get it.

Nervous about an upcoming interview? Unsure how to write a new resume?

Visit the Hays Career Advice section to learn top tips to help you stand out from the crowd when job hunting.

Hays is an Equal Opportunity Employer including disability/veteran.

In accordance with applicable federal and state law protecting qualified individuals with known disabilities, Hays U.S. Corporation will attempt to reasonably accommodate those individuals unless doing so would create an undue hardship on the company. Any qualified applicant or consultant with a disability who requires an accommodation in order to perform the essential functions of the job should call or text 813.336.5570

Drug testing may be required; please contact a recruiter for more information. #1141732

Summary

Job Type
Permanent
Industry
Pharmaceuticals
Location
Cambridge
Specialism
Pharma
Pay
250,000 - 295,000
Ref:
1141732