MFMatthew Fink
@matthewfink
Experienced manager in clinical research with a focus on oncology.
United StatesWhat I'm looking for
I am a Manager in Study Start-Up with over a decade of experience in clinical research, specializing in regulatory compliance and data-driven strategies. My journey has been marked by a commitment to enhancing team collaboration and project delivery, particularly in the fields of Oncology and Cell Therapy Research. I am passionate about innovative problem-solving and dedicated to exceeding timelines and milestones to bring potential therapies to patients faster.
At Bristol Myers Squibb, I independently manage study, country, and site-level deliverables, ensuring timely milestones with both internal and external partners. My role includes planning and developing strategies for start-up activities that enhance recruitment and trial success. I have also taken on a leadership role as Co-Chair of the IRB SME Team, where I authored the Global IRB SOP and managed the RCO US Central IRB preferred vendor selection process.
My experience extends to mentoring new hires through structured training sessions, fostering a supportive environment that enhances team collaboration and performance. I am dedicated to streamlining communication between internal teams and external partners to minimize risk and ensure compliance with FDA and GCP guidelines.
Experience
Work history, roles, and key accomplishments
Manager, Study Start-up Specialist
Bristol Myers Squibb
Apr 2022 - Present (3 years 2 months)
Independently managed study, country, and site-level deliverables, ensuring timely milestones with internal and external partners. Developed strategies for start-up activities, enhancing recruitment and trial success. Co-chaired the IRB SME Team and authored the Global IRB SOP, managing RCO US Central IRB preferred vendor selection.
Senior Study Start-up Specialist
Bristol Myers Squibb
Jan 2021 - Present (4 years 5 months)
Supported the study start-up process, ensuring timely initiation of clinical trials. Collaborated with cross-functional teams to meet regulatory requirements and project milestones.
Study Start-up Specialist II
DOCS Global
Mar 2020 - Present (5 years 3 months)
Managed critical aspects of clinical study initiation, focusing on site activation and document submission. Ensured adherence to global regulatory guidelines and internal standard operating procedures.
Project Manager - Cardiology
Hospital of UPenn
May 2016 - Present (9 years 1 month)
Oversaw cardiology research projects, coordinating resources and timelines to achieve study objectives. Facilitated communication between research teams, clinicians, and external partners.
Student Clinical Research Assistant – Cardiology
Hospital of UPenn
May 2014 - Present (11 years 1 month)
Assisted with data collection and patient recruitment for cardiology clinical trials. Supported research staff in maintaining study documentation and ensuring compliance with protocols.
Education
Degrees, certifications, and relevant coursework
UPUniversity of Pennsylvania
Bachelor of Arts, Biological Basis of Behavior
Focused on the biological basis of behavior, gaining a foundational understanding of the biological underpinnings of behavior. Developed skills in scientific inquiry and research methodologies relevant to clinical studies.
Tech stack
Software and tools used professionally
Availability
Location
United StatesAuthorized to work in
Job categories
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