Daniel Powers

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

Experience

1. Senior Vice President Clinical Development

   C4 Therapeutics, Inc.

   Apr 2024 — Present · 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

  2001 — 2002

• National Naval Medical Center

  Internal Medicine PGY-1,2, Internal Medicine Residency Program

  1997 — 2001

• University of Medicine and Dentistry of New Jersey - School of Osteopathic Medicine

  Doctor of Osteopathic Medicine - D.O., Medicine

  1993 — 1997

Skills

• Clinical Research
• Ehr
• Business Strategy
• Pharmaceutical Industry
• Data Analysis
• Emr
• Cardiology
• Building Strong Business Relationships
• Strategic Planning
• Consulting
• Marketing
• New Business Development
• Healthcare Management
• Strategy
• Diabetes
• Healthcare
• Business Development
• Healthcare Information Technology
• Hipaa
• Management Consulting
• Medicine
• Social Media Measurement
• Social Media Marketing
• Cross-Functional Team Leadership
• Healthcare Consulting
• Community Engagement
• Marketing Strategy
• Leadership
• Management
• Team Building
• Internal Medicine
• High Organizational Skills
• Multi Tasking
• Hospitals
• Communication Skills
• Start-Ups