Senior Level Clinical Oncology Specialist Jobs
Senior level clinical oncology specialist jobs place experienced professionals in charge of treatment protocol oversight, multidisciplinary team leadership, and the clinical outcomes that define a program's standard of care. Roles are concentrated across Staffing & Recruiting, Biotechnology & Pharmaceuticals, and Education, with a mix of on-site, hybrid, and remote positions, and employers like Jobot, Systimmune, and Allogene Therapeutics hiring at this level now.
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We are seeking a highly skilled and motivated Senior Global Director, Clinical Project Management (CPM) to join our dynamic team. The successful candidate will oversee and coordinate global clinical trials from initiation through to completion. This role involves ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. The Senior Global Director, Clinical Project Management, will play a critical role in delivering high-quality data and ensuring the success of clinical studies.
Key Responsibilities
- Oversee the planning and execution of global clinical trials
- Develop and implement study protocols, timelines, and budgets.
- Manage all aspects of clinical trial operations, including site selection, initiation, monitoring, and closeout.
- Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines.
- Coordinate with cross-functional teams, including investigators, vendors, and regulatory bodies.
- Monitor trial progress and manage data collection to ensure accuracy and integrity.
- Identify and mitigate project risks
- Oversee a team of regional CPMs, CRAs and CTAs.
- Ensure the preparation and submission of regulatory documents are compliant with local regulatory standards and maintained per good clinical practice.
- Conduct regular meetings with study teams and provide updates to stakeholders.
- Coordinate with external vendors and partners involved in the trial
- Support development of key process initiatives and SOPs internally
- Oversee vendors supporting trial execution
Qualifications
- Bachelor’s degree in Life Sciences, Nursing, or a related field.
- Minimum of 15 years of experience in Clinical Trial Management, including demonstrated people leadership and direct line management experience.
- Strong experience working on early phase studies required, late phase studies experience is a plus.
- Strong understanding of GCP and regulatory requirements.
- Excellent organizational and project management skills.
- Proven ability to lead cross-functional teams and manage multiple priorities.
- Strong communication and interpersonal skills.
- Ability to work collaboratively in a team-oriented environment
- Flexibility and adaptability to changing priorities and workload
- Princeton NJ hybrid, 3 days in office
- Overnight travel ~25%
The expected base salary range for this position is $220,000 - $280,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
We are seeking a highly skilled and motivated Senior Global Director, Clinical Project Management (CPM) to join our dynamic team. The successful candidate will oversee and coordinate global clinical trials from initiation through to completion. This role involves ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. The Senior Global Director, Clinical Project Management, will play a critical role in delivering high-quality data and ensuring the success of clinical studies.
Key Responsibilities
- Oversee the planning and execution of global clinical trials
- Develop and implement study protocols, timelines, and budgets.
- Manage all aspects of clinical trial operations, including site selection, initiation, monitoring, and closeout.
- Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines.
- Coordinate with cross-functional teams, including investigators, vendors, and regulatory bodies.
- Monitor trial progress and manage data collection to ensure accuracy and integrity.
- Identify and mitigate project risks
- Oversee a team of regional CPMs, CRAs and CTAs.
- Ensure the preparation and submission of regulatory documents are compliant with local regulatory standards and maintained per good clinical practice.
- Conduct regular meetings with study teams and provide updates to stakeholders.
- Coordinate with external vendors and partners involved in the trial
- Support development of key process initiatives and SOPs internally
- Oversee vendors supporting trial execution
Qualifications
- Bachelor’s degree in Life Sciences, Nursing, or a related field.
- Minimum of 15 years of experience in Clinical Trial Management, including demonstrated people leadership and direct line management experience.
- Strong experience working on early phase studies required, late phase studies experience is a plus.
- Strong understanding of GCP and regulatory requirements.
- Excellent organizational and project management skills.
- Proven ability to lead cross-functional teams and manage multiple priorities.
- Strong communication and interpersonal skills.
- Ability to work collaboratively in a team-oriented environment
- Flexibility and adaptability to changing priorities and workload
- Princeton NJ hybrid, 3 days in office
- Overnight travel ~25%
The expected base salary range for this position is $220,000 - $280,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
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Senior Level Clinical Oncology Specialist Jobs: Frequently Asked Questions
How do I get a senior level clinical oncology specialist job?
Employers at this level look for demonstrated ownership of complex oncology cases, experience guiding junior clinicians or specialists, and a record of contributing to protocol development or quality improvement initiatives. Candidates who can speak to program-level impact, cross-functional collaboration with oncology teams, and specialized expertise in a particular cancer type or treatment modality tend to stand out in competitive searches.
Which companies hire senior level clinical oncology specialists?
Companies hiring senior level clinical oncology specialists right now include Jobot, Systimmune, and Allogene Therapeutics, based on current listings on Migrate Mate as of November 2026. Hiring at this level comes primarily from academic medical centers, large health systems, specialty cancer institutes, and pharmaceutical or biotech organizations running clinical trial programs.
Are there remote senior level clinical oncology specialist jobs?
Yes, though remote availability depends heavily on the specific function within oncology. About 80% of senior level clinical oncology specialist openings are remote or hybrid as of November 2026, with fully remote roles more common in medical affairs, clinical operations, and oncology education than in direct patient care or on-site clinical practice settings.
What makes a clinical oncology specialist role senior level?
Senior level roles are defined by scope and accountability rather than task execution. At this stage, professionals own clinical programs or service lines, set standards for patient care delivery, mentor mid-level and early-career colleagues, and contribute to strategic decisions around treatment pathways or departmental growth. The expectation shifts from following protocols to shaping them.
Which industries hire the most senior level clinical oncology specialists?
Senior Level clinical oncology specialist roles concentrate in Staffing & Recruiting, Biotechnology & Pharmaceuticals, and Education, based on current listings on Migrate Mate as of November 2026. These sectors drive hiring at this level because they operate large patient populations, invest heavily in oncology research and treatment innovation, and require experienced specialists to lead both clinical and programmatic functions.