Summary
Overview
Work History
Education
Skills
Websites
Therapeutic Area | Clinical Trials Experience
Core Oncology Research Focus
Systems Experience
Interests
Timeline
Generic

LEE ADKINS

RALEIGH

Summary

  • Dedicated Pharmaceutical Research Management professional with:
  • A direct, goal-oriented, transparent and supportive management style
  • Cooperative, relationship-centered communication style
  • 25+ years of combined, cross-functional, industry experience in advancing roles with increased leadership and oversight responsibilities; including
  • Full-scope Phase I – IV Clinical Monitoring, Project and Program Management experience
  • Oversight experience of study operations, timelines and budgets ranging from $450K to $24M
  • 14+ years of direct Early Phase Oncology experience
  • 3+ years as Project Director/Program Lead, dedicated to EPO Biotech Client Management
  • 3+ years of Line Management experience, under direct and matrix models; and
  • 6+ years in Clinical Monitoring and Clinical Team Lead roles.

Experienced with strategic planning, project management, and stakeholder communication. Utilizes these skills to enhance operational efficiency and drive team success. Track record of effective leadership in high-stakes environments.

Results-driven professional with extensive experience in leadership and strategic oversight. Adept at driving organizational success through effective team collaboration and dynamic problem-solving. Recognized for adaptability and keen focus on achieving objectives.

Qualified [Desired Position] with proven background in strategic planning and project management. Successfully led cross-functional teams to deliver high-impact initiatives. Demonstrated excellence in stakeholder communication and operational efficiency.

Professional leader with extensive experience in driving strategic initiatives and fostering effective team collaboration. Strong background in project management, budget oversight, and stakeholder engagement, ensuring organizational goals are met efficiently. Known for adaptability, reliability, and focus on achieving impactful results. Skilled in leveraging data-driven insights, optimizing processes, and mentoring teams to excel in dynamic environments.

Highly organized and self-motivated professional experienced in project management, team development and process improvement. Skilled in developing and implementing strategies to increase efficiency and performance. Passionate about driving business growth and creating positive work environment.

Encouraging manager and analytical problem-solver with talents for team building, leading and motivating, as well as excellent customer relations aptitude and relationship-building skills. Proficient in using independent decision-making skills and sound judgment to positively impact company success. Dedicated to applying training, monitoring and morale-building abilities to enhance employee engagement and boost performance.

Collaborative leader partners with coworkers to promote engaged, empowering work culture. Documented strengths in building and maintaining relationships with diverse range of stakeholders in dynamic, fast-paced settings.

Innovative and goal-oriented Management professional committed to [Area of expertise]. Dedicated team player skilled at mediation and conflict resolution. Drives company growth through [Action].

Proficient [Job Title] delivering encouragement and feedback to help employees be successful. Energetic professional with great poise. Well-trained in [Skill].

Dedicated [Industry] professional with a history of meeting company goals utilizing consistent and organized practices. Skilled in working under pressure and adapting to new situations and challenges to best enhance the organizational brand.

Overview

27
27
years of professional experience

Work History

Associate Director - Clinical Project Management

CTI Clinical Trial and Consulting
09.2024 - 04.2025
  • Primary oversight and relationship manager for 3 Sponsors
  • Functional management of 6 Sr. PMs and PMs to established financial, timeline, and quality metrics
  • BD and Operations support via RFP review, risk assessment and budgetary input, and BDM preparations and presentations
  • Line Management and Onboarding of 5 Sr. PMs and PMs
  • Mentor to 2 Sr. PMs
  • Remote
  • Led cross-functional teams to develop and implement strategic initiatives enhancing organizational efficiency.
  • Oversaw budgeting processes, ensuring alignment with organizational goals and effective resource allocation.
  • Mentored junior staff, fostering professional development and enhancing team productivity through knowledge sharing.
  • Led teams of up to [Number] personnel, supervising daily performance as well as training and improvement plans.
  • Prioritized tasks and allocated resources appropriately to keep teams focused and productive.
  • Managed cross-functional teams for multiple large-scale projects, successfully completing each on time and within budget constraints.
  • Mentored junior staff members, providing guidance on professional development opportunities and career progression paths within the company.
  • Used industry expertise, customer service skills and analytical nature to resolve customer concerns and promote loyalty.
  • Defined clear targets and objectives and communicated to other team members.

Project Director

Syneos Health
12.2020 - 04.2024
  • Primary oversight and relationship manager, for 4 - 6 Sponsors
  • Functional management of 7 Sr. PMs, PMs, and Associate PMs to established financial, timeline, and quality metrics
  • BD and Operations support via RFP review, risk assessment and budgetary input, and BDM preparations and presentations
  • Mentor to 2 Sr. PMs and 1 PMs
  • Remote

Sr. Project Manager

MedSource
01.2017 - 12.2020
  • Retained all responsibilities of prior PM/Sr. PM positions and oversaw:
  • 4 Phase I/Ib, FIH, Oncology trials
  • 2 CTLs, 6 CRAs, and 2 supporting CTAs
  • 86% BDM to Award Win rate
  • Remote

Sr. Project Manager

Chiltern Intl.
03.2014 - 12.2016
  • 65 site multi-national Phase III bladder cancer trial
  • 2 CTLs, 7 CRAs, and 2 supporting CTAs
  • 66% BDM to Award Win rate
  • Nominated for 2014 CEO Award by Sr. Project Director
  • Remote

Project Manager, Clinical Operations

Ockham Oncology
11.2012 - 03.2014
  • 5 Phase I-Ib solid tumor studies
  • 3 Lead CRAs, 9 CRAs, and 3 supporting CTAs
  • 3 different PK/PD/Bioanalysis vendors and 2 EDC platforms
  • Nominated for 2013 CEO Award by Sr. Project Director
  • Remote

Manager, Drug Development

Chelsea Therapeutics
01.2011 - 11.2012
  • Full study oversight of 2 Phase II/III studies
  • Protocol, ICF, and CRF design
  • QA and clinical review of TLFs and CSRs in support of a New Drug Application (NDA) submission
  • Supported 4 Investigator Initiated studies with KOLs

Manager, Strategic Site Relationships

Quintiles, Inc.
06.2008 - 05.2010

Associate Clinical Scientist

Quintiles, Inc.
02.2006 - 06.2008

Sr. CRA – Clinical Team Lead

Quintiles, Inc.
03.2005 - 02.2006

Sr. CRA – Site Monitor

Quintiles, Inc.
02.2003 - 03.2005

Clinical Research Associate

Quintiles, Inc.
02.2000 - 02.2003

Clinical Trials Associate

Quintiles, Inc.
06.1998 - 02.2000

Education

Bachelor of Science - Biology

University of North Carolina
Chapel Hill, NC

Skills

  • Project/Program Management
  • Risk Assessment and Mitigation
  • Conflict Resolution
  • Relationship Management
  • Change Management
  • Budget Development
  • Quality Management
  • Communication
  • Clinical Monitoring
  • Line Management
  • Problem Solving
  • Business Development
  • Clinical project management
  • Relationship management
  • Cross-functional leadership
  • Budget management
  • Risk assessment
  • Resource allocation
  • Team mentoring
  • Operational efficiency
  • Strategic planning
  • Proposal development
  • Quality assurance
  • Regulatory compliance
  • Clinical trial oversight
  • Performance metrics analysis
  • Vendor management
  • Stakeholder engagement
  • Process improvement
  • Timeline management
  • Training and development
  • Data analysis
  • Project management
  • Strategic leadership
  • Analytical thinking
  • Coaching and mentoring
  • Relationship building
  • Decision-making
  • Team collaboration and leadership
  • Key relationship management
  • Operations management
  • MS office
  • Budget development
  • Work Planning and Prioritization
  • Administrative support
  • Performance evaluations
  • Verbal and written communication
  • Recruiting and interviewing
  • Project methodology
  • Reporting and documentation
  • Fiscal oversight
  • Program coordination
  • Risk analysis
  • Task delegation

Therapeutic Area | Clinical Trials Experience

  • Phase I Advanced Pancreatic Cancer [CRA]
  • Solid Tumors [CRA, LCRA, PM]
  • Multiple Myeloma [PM]
  • NSCLC [PM]
  • Glioblastoma and Glioma [PM]
  • Ovarian – Advanced, recurrent, platinum-resistant [CRA, LCRA, PM]
  • Hormone Insufficient Male Hot Flashes [CRA]
  • QTc (thorough ECG) trial [PM]
  • Phase I (Specialty) First in Human – Oncology [CRA, PM]
  • Bioequivalence [PM]
  • Phase II/III Non-muscle Invasive Bladder Cancer [PM]
  • Parkinson’s Disease [PM]
  • Superficial Bladder Cancer [CRA]
  • Advanced Urinary Tract Cancer [CRA/LCRA]
  • Pancreatic Cancer [CRA, LCRA]
  • Intracerebral Hemorrhagic Stroke [CRA]
  • Rheumatoid Arthritis [LCRA]
  • Type 2 Diabetes Mellitus [LCRA]
  • Phase IV Hepatitis C [CRA, LCRA]

Core Oncology Research Focus

  • Early Phase Oncology
  • Immuno-Oncology
  • Monoclonal Antibodies
  • First in Human Trials
  • Solid Tumors
  • Checkpoint Inhibitors
  • Basket Trials
  • Antibody Drug Candidates (ADCs)
  • Adaptive Design Protocols
  • Chimeric Antigen Receptors (CAR-T)

Systems Experience

  • EDCs INFORM RAVE
  • IBM/MERGE/eCOS DataTrial (NowEDC)
  • ETMFs Veeva Vault TransPerfect (Trial Interactive)

Interests

  • Music
  • Volunteering for community initiatives to give back to local communities and make a positive impact
  • Mindfulness Practices
  • Volunteer Work

Timeline

Associate Director - Clinical Project Management

CTI Clinical Trial and Consulting
09.2024 - 04.2025

Project Director

Syneos Health
12.2020 - 04.2024

Sr. Project Manager

MedSource
01.2017 - 12.2020

Sr. Project Manager

Chiltern Intl.
03.2014 - 12.2016

Project Manager, Clinical Operations

Ockham Oncology
11.2012 - 03.2014

Manager, Drug Development

Chelsea Therapeutics
01.2011 - 11.2012

Manager, Strategic Site Relationships

Quintiles, Inc.
06.2008 - 05.2010

Associate Clinical Scientist

Quintiles, Inc.
02.2006 - 06.2008

Sr. CRA – Clinical Team Lead

Quintiles, Inc.
03.2005 - 02.2006

Sr. CRA – Site Monitor

Quintiles, Inc.
02.2003 - 03.2005

Clinical Research Associate

Quintiles, Inc.
02.2000 - 02.2003

Clinical Trials Associate

Quintiles, Inc.
06.1998 - 02.2000

Bachelor of Science - Biology

University of North Carolina
LEE ADKINS