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Senior Clinical Team Manager (Prin.) - Hemonc

8+ years
Not Disclosed
10 Nov. 3, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.