Daniel Powers
Senior Vice President Clinical Development @C4 Therapeutics, Inc.
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WORK HISTORY
Senior Vice President Clinical Development @C4 Therapeutics, Inc.
Watertown, MA, US
Responsible for medical and clinical oversight and clinical trial execution of multiple early-stage programs in protein degradation, including BRAF V600X mutant cancers (melanoma, CRC, NSCLC) and IKZF1/3 (multiple myeloma, NHL). • Accountable for driving development strategy towards Regulatory success, from preliminary breakthrough designation to accelerated and full approval; adapting to emerging data and leading multiple cross-functional teams through the development of adaptive study concepts.• Developed a collaborative and creative approach to problem-solving within teams that valued inclusion while optimizing decision-making and team-effectiveness.• Built an integrated clinical development department, expanded medical and clinical science teams, and restructured the governance process.• Provided medical and clinical leadership to translational science/medicine, data analysis and interpretation, US and global regulatory interactions, clinical operations, quality assurance, supply chain management, and others.• Served as the spokesperson for interactions with investigators, KOLs, consultants, and health authorities. • Reviewer, signatory, and /or author for clinical development plans, protocols, IBs, DSUR, Regulatory documents, publications.
EDUCATION
UMass Boston
Bachelor's Degree, Chemistry
Yale-New Haven Hospital, Saint Raphael Campus
Internal Medicine PGY-3, Internal Medicine Residency Program
National Naval Medical Center
Internal Medicine PGY-1,2, Internal Medicine Residency Program
University of Medicine and Dentistry of New Jersey - School of Osteopathic Medicine
Doctor of Osteopathic Medicine - D.O., Medicine
SKILLS
ABOUT DANIEL POWERS
Experienced Clinical Development and Medical Affairs pharmaceutical executive, physician researcher, clinician. Demonstrated success at designing and managing multiple phase I-IV clinical trials. Extensive leadership experience managing cross-functional teams and direct reports in both clinical development and medical affairs. Experienced in heme and solid tumor malignancies. Excellent communicator and builder of relationships with KOLs. Proven ability to develop careers of direct reports.Core Strengths:• Design and execute forward-thinking clinical trials that provide relevant data within the treatment landscape• Provide expert medical guidance across the spectrum of clinical development and medical affairs, from medical monitoring to study design and execution, from publications to KOL engagement • Develop and foster cross-functional engagement • Effectively manage CROs and consultants to balance costs and optimize delivery schedules• Develop enduring and productive relationships with KOLs and investigators• Purposefully develop and mentor direct reports to achieve high promotion rates
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