Jeremy James Thurmon
Hurst,USA
Summary
Project management professional with track record of delivering high-impact projects in diverse environments. Adept at driving project timelines and ensuring quality outcomes through strategic planning and execution. Highly collaborative, adaptable, and committed to team success and client satisfaction.
Overview
22
22
years of professional experience
Work History
Project Manager II
Fortrea (formerly Labcorp DD/Covance)
09.2020 - 03.2025
- Successfully met challenges in scope, time, and budget by developing strategic management plans, resulting in enhanced client satisfaction and boosted future business prospects.
- Improved potential for repeat business by serving as the primary client contact, enhancing operational excellence and client relations.
- Enhanced cross-functional collaboration and project success by leading diverse core project teams to achieve objectives.
- Maintained high client satisfaction by ensuring compliance with ICH GCP and regulatory standards, overcoming audit challenges.
- Managed complex project issues by acting as the escalation point, maintaining project momentum and building stakeholder trust.
- Demonstrated strategic budget management by realigning project delivery strategies to meet 85% of financial performance targets.
- Ensured project success by aligning scope, schedule, and cost challenges with contractual and financial targets.
- Maintained stakeholder alignment by introducing change control processes to address evolving requirements.
- Enhanced overall project quality through quality control and risk assurance activities, meeting regulatory and client requirements.
- Achieved effective risk management in project protocols by formulating mitigation strategies for complex execution risks.
- Improved outcomes by managing variances in project plans, enhancing team performance.
- Efficiently met client metrics through targeted process improvements by developing and maintaining key performance indicators.
- Ensured consistent progress and resource availability by defining and managing resource requirements in challenging environments.
- Improved project acquisition potential by 10% by contributing strategic insights during bid defense presentations.
- Ensured successful project completion by monitoring project progress against financial milestone aligning with financial systems.
Senior Project Manager
Total Clinical Trial Management (TCTM)
11.2014 - 09.2020
- Increased company visibility and win rates by navigating competitive challenges in strategic project proposals.
- Aligned projects with timelines and objectives by addressing planning and execution challenges to provide operational support.
- Achieved a 20% increase in recruitment by optimizing patient recruitment programs, enhancing study enrollment and meeting deadlines.
- Ensured timely and budget-compliant deliverables by negotiating favorable vendor contracts under challenging conditions.
- Maintained compliance and transparency with investigator sites through diligent budget and payment management.
- Ensured consistent study quality across projects by directing clinical personnel in investigator identification and training.
- Increased efficiency in therapeutic areas by leading the design and development of clinical study protocols and CRFs.
- Ensured adherence to safety, consistency, and budget regulations by implementing clinical trials with cross-functional teams.
- Achieved successful outcomes by facilitating clinical trial activities, improving trial efficiency by 15%.
- Ensured quality and consistency in documentation by contributing to the preparation of clinical program documents.
- Showcased professional growth through career advancement by accepting increased responsibilities in complex settings.
- Maintained schedules and data integrity by providing support as a traveling CRA during resource shortages.
Medical Safety Scientist
Alcon Laboratories
10.2009 - 05.2014
- Improved documentation processes and streamlined operations by 20% by developing and reviewing clinical trial protocols and SOPs.
- Maintained study integrity through timely evaluation of safety data to resolve queries during complex trial phases.
- Ensured comprehensive project oversight by coordinating closely with safety physicians on tight timelines.
- Contributed to successful audits and regulatory compliance through the preparation of high-quality safety data documents.
- Advanced protocol activities and coordinated IDE preparation related to safety sections.
- Expedited product registration activities by developing safety overviews for PMA submissions and agency responses.
- Maintained ongoing regulatory compliance by staying updated with safety surveillance guidelines.
- Played an integral role in overall project success by contributing to team success during protocol phases.
- Drove critical discussions and decision-making by leading franchise team meetings in management's absence.
- Expanded product reach by 30% through significant contribution to the approval of AcrySof ReSTOR +2.5 D Intraocular Lens.
Clinical Research Coordinator
U.S. Department of Veterans Affairs Hospital
01.2007 - 01.2009
Clinical Data Specialist
UT Southwestern Medical Center
01.2006 - 01.2007
Research Assistant II
UT Southwestern Medical Center
01.2003 - 01.2005
Education
Masters Degree - Healthcare Administration (MHA)
University of Texas at Arlington
Arlington, TXBachelor of Science - Biology
Abilene Christian University
Abilene, TXSkills
- Clinical Study Management (Phase II and III)
- Regulatory Affairs Expertise
- Global Regulatory Strategy
- Inspection Readiness in Clinical Research
- Strategic Partnership Management
- Risk Assessment and Mitigation
- Operational Strategy Development
- Strategic Budget Planning & Management
- Cross-functional Team Leadership in Clinical Settings
- Vendor Oversight and Agency Inspection Preparedness
- CRO Experience
- Technical Skills: MS Office Suite
- MS Project
- SAP
- SPSS
- Medidata Rave
- Smartsheet
- SharePoint
Therapeutic Experience
Fortrea
- Ophthalmology: Diabetic Retinopathy/nAMD (Phase II)
- Ophthalmology: Wet AMD (Phase II)
- Obstetrics/Gynecology: Abnormal Uterine Bleeding (Phase III)
- Hematology: Rare Disease (Phase III)
TCTM
- Ophthalmology: Acute Angle Glaucoma/Raised IOP (Phase III)
- Gastroenterology: Inflammatory Bowel Disease (Phase III)
- Dermatology: Rosacea (Phase III)
Alcon Laboratories
- Ophthalmology Device: Surgical Intraocular Lens - IOL (Phase III)
- Ophthalmology: Diabetic Retinopathy/Wet AMD (Phase III)
VA Hospital
- Anesthesiology: Acute Pain Post-Operative Pain (Phase III)
Publications
- Chandramouli P. Iyer, Brian D. Robertson, Fima Lenkovsky, Sergio Huerta, Edward Livingston, Jeremy J. Thurmon. Gastric bypass and On-Q pump: Effectiveness of Soaker Catheter system on recovery of bariatric surgery patients. Surgery for Obesity and Related Diseases - 4March 2010 (Vol. 6, Issue 2, Pages 181-184, DOI: 10.1016/j.soard.2009.08.008).
- Hommel JD, Trinko R, Sears RM, Georgescu D, Liu ZW, Gao XB, Thurmon JJ, Marinelli M, DiLeone CY06. Leptin receptor signaling in midbrain dopamine neurons regulates feeding. Neuron. 2006 Sep 21;51(6):801-10.
Timeline
Project Manager II
Fortrea (formerly Labcorp DD/Covance)
09.2020 - 03.2025
Senior Project Manager
Total Clinical Trial Management (TCTM)
11.2014 - 09.2020
Medical Safety Scientist
Alcon Laboratories
10.2009 - 05.2014
Clinical Research Coordinator
U.S. Department of Veterans Affairs Hospital
01.2007 - 01.2009
Clinical Data Specialist
UT Southwestern Medical Center
01.2006 - 01.2007
Research Assistant II
UT Southwestern Medical Center
01.2003 - 01.2005
Masters Degree - Healthcare Administration (MHA)
University of Texas at Arlington
Bachelor of Science - Biology
Abilene Christian University
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