Job Title:
Senior Clinical Team Manager (Principal) – Hematology/Oncology
Location:
Remote – North Carolina, United States
Job ID:
R-01327955
Job Type:
Full-Time
Category:
Clinical Research
Work Arrangement:
Fully Remote
Work Schedule:
Standard (Monday – Friday)
About Thermo Fisher Scientific
At Thermo Fisher Scientific, our colleagues in Clinical Research Services are dedicated to advancing global healthcare by accelerating the development of life-saving therapies. Through our PPD® clinical research portfolio, we combine world-class scientific, medical, and operational expertise to deliver excellence in every study phase.
About the Role
We are seeking an accomplished Senior/Principal Clinical Team Manager (CTM) to lead and manage global clinical research projects within the Hematology/Oncology (HemOnc) therapeutic area.
This role provides a unique opportunity to direct impactful studies that influence the development of treatments for complex cancers and blood disorders.
As a CTM, you will oversee clinical operations, ensure compliance with regulatory standards, and drive successful completion of clinical trials — from study start-up to closeout — within defined timelines and budgets.
Therapeutic Scope
You will work on oncology trials across multiple indications, including:
Ovarian Cancer
Sickle Cell Disease
Non-Hodgkin’s Lymphoma
Multiple Myeloma
Glioma
Head and Neck Cancer
Pancreatic Cancer
Prostate Cancer
Non-Small Cell Lung Cancer
Breast and Colorectal Cancer
Radiopharmaceuticals
Cell and Gene Therapy / CAR-T
Key Responsibilities
Clinical Project Leadership
Lead all clinical operational and quality aspects of assigned studies (moderate to high complexity).
Ensure compliance with ICH-GCP, study protocols, and corporate policies.
Develop and implement clinical monitoring tools and documentation, such as Monitoring Plans and Guidelines.
Oversee Trial Master File (TMF) setup, organization, and quality.
Support protocol development, CRF design, and informed consent template preparation.
Cross-Functional Collaboration
Partner closely with the Project Manager to ensure clinical deliverables align with project goals.
Collaborate with functional leads (data management, safety, regulatory, and medical teams).
Contribute to bid defenses, client meetings, and project hand-offs.
Team Management and Training
Manage and mentor Clinical Management team members.
Provide training, guidance, and oversight to ensure high-quality clinical performance.
Conduct Accompanied Field Visits (AFVs) as needed to ensure monitoring quality and consistency.
Study Execution and Oversight
Drive achievement of final clinical deliverables — including clean data and evaluable patients.
Track and monitor timelines, metrics, and budgets; identify risks and implement mitigation plans.
Ensure adherence to project scope and maintain profitability.
Oversee start-up activities, regulatory submissions, and essential document quality.
Client and Site Interaction
Serve as a primary contact for sponsors on clinical aspects.
Address site-level issues related to protocol adherence, CRF completion, and patient participation.
Process and Quality Improvement
Identify opportunities to enhance efficiency, consistency, and quality within clinical operations.
Participate in corporate process improvement initiatives and cross-functional working groups.
Education and Experience
Required
Bachelor’s degree (Life Sciences, Medicine, Pharmacy, or related discipline) or equivalent qualification.
Minimum 8 years of experience in clinical research, including experience in project or team leadership roles.
Preferred
Advanced degree (MSc/PharmD/PhD/MD) in a related field.
Proven record of leading global oncology and hematology trials across multiple indications.
Experience with cell and gene therapy or CAR-T trials preferred.
Demonstrated success in managing cross-functional teams and complex, multi-country studies.
Knowledge, Skills, and Abilities
Strong leadership, mentoring, and motivational abilities.
Excellent project planning, time management, and organizational skills.
Ability to communicate complex scientific and operational information clearly.
Expertise in ICH-GCP, FDA regulations, and global clinical research standards.
Strong financial acumen for budgeting, forecasting, and resource allocation.
Effective decision-making, escalation, and risk management capabilities.
Proficiency in Microsoft Office Suite and clinical trial management systems (CTMS).
Experience in change management and cross-functional coordination in a matrix organization.
Exceptional attention to detail and commitment to quality.
Working Environment and Travel
Remote, office-based work environment.
Requires strong communication with diverse teams across regions.
Ability to remain stationary for long periods.
Exposure to digital and data systems common in clinical operations.
May require travel up to 20%, including domestic and international trips by air, train, or automobile.
Possible exposure to healthcare or laboratory settings during site visits.
Core Values
At Thermo Fisher Scientific, our culture is guided by our 4i Values:
Integrity – Innovation – Intensity – Involvement
Why Join Us
Be part of a global leader in contract research and clinical development.
Work on transformative oncology therapies that save lives.
Enjoy a people-first culture that prioritizes growth, balance, and inclusion.
Access to competitive compensation, annual bonuses, healthcare, and career development programs.
Mission Statement
“To enable our customers to make the world healthier, cleaner, and safer.”
If you are driven by purpose and passionate about advancing oncology research, we invite you to apply and become part of a team that’s shaping the future of healthcare.
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Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
Atlanta | Augusta | Rome |Maine :
Bangor | Brewer |New Jersey :
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Concord | Lumberton | North Carolina |Michigan :
Detroit | Houghton Lake | Macomb | Southfield |North Dakota :
Dickinson |Minnesota :
Duluth | Eden Prairie | Fridley | Hibbing | Maple Grove | Minneapolis and St. Paul, Minnesota. | Minnetonka | St.Paul |Kentucky :
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Frank Scottile Blvd |Missouri :
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Germany | GErmany |Lower Saxony :
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Bulgaria | Vedant |Denmark :
Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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China | Quarry Bay |Liaoning :
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Arkansas | Remote Australia |New South Wales :
Ballina | Sydney |Republic of Western Australia :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
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Yavne | Kfar Saba | Netanya | Be'Er Sheva | Tel Aviv |Remote :
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King Abdullah Economic City | Khulais | Riyadh | Rabigh | Najran | Jeddah |Kuala Lumpur :
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Kyiv |Lima Region :
Lima |France :
Lyon | Paris |South Africa :
Midrand | South Africa |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
Sarajevo |Singapore :
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