Contractual Research Study Monitor Jobs (NOW HIRING)

The Research Study Manager oversees day-to-day clinical research operations across multiple oncology sites, ensuring high-quality execution of clinical trials, regulatory compliance, and effective coordination of research activities. This role supervises clinical research coordinators and workflow, partners closely with physicians and site teams, and drives the growth of oncology clinical research programs through strong leadership, operational excellence, and strategic support for study selection, recruitment, and data management.

• Oversee the day-to-day clinical research operations for assigned oncology locations, ensuring smooth and efficient conduct of clinical trials.
• Supervise clinical research coordinators and other team members, including assigning workload, monitoring performance, and supporting professional development.
• Manage and coordinate disease-specific research groups, ensuring appropriate staffing, prioritization, and alignment with study requirements.
• Partner with physicians to educate them on available studies, assist in selecting appropriate trials, and explain feasibility considerations for each site.
• Collaborate with site teams to oversee oncology research activities, meeting teams where they are in their processes and helping them align with central research standards.
• Support physicians in identifying and selecting trials that match patient populations, site capabilities, and institutional priorities.
• Review and interpret clinical trial protocols, ensuring that research staff understand study requirements, timelines, and operational expectations.
• Develop, refine, and support site-level screening processes to improve patient identification, enrollment, and retention in oncology trials.
• Communicate and promote services that support and enable the growth of clinical research, particularly in recruitment, retention, coordination of research, and data management.
• Ensure adherence to all regulatory requirements and institutional policies related to clinical research, including documentation, reporting, and compliance activities.
• Coordinate with regulatory, data management, and other research support teams to maintain high standards of data quality and regulatory readiness.
• Monitor study progress, identify operational challenges, and implement process improvements to enhance efficiency and study performance.
• Foster a collaborative, supportive environment among clinical research coordinators, physicians, and other stakeholders involved in oncology research.

• Demonstrated experience supervising clinical research coordinators and managing workflow in a clinical research setting.
• Prior hands-on oncology clinical research experience, including work as a Clinical Research Coordinator (CRC).
• 5–7 years of oncology experience in clinical research or related roles.
• At least 2 years of supervisory experience leading research staff or clinical operations teams.
• Strong understanding of clinical trial operations, including coordination, data management, and regulatory compliance.
• Ability to interpret and understand clinical trial protocols and translate requirements into operational plans.
• Proven experience in clinical research roles such as Clinical Research Coordinator, Clinical Research Supervisor, Clinical Operations professional, or Research Program Manager.
• Bachelor’s degree in a science discipline.
• Effective communication skills to partner with physicians, site teams, and cross-functional research staff.
• Ability to develop and support patient screening and enrollment strategies for oncology trials.

• Experience working within an oncology-focused research environment, such as a cancer institute or comprehensive cancer center.
• Background in coordinating or supervising multiple disease-specific research groups or programs.
• Experience collaborating with regulatory affairs teams and clinical research management to support compliant and efficient trial conduct.
• Capability to influence and align site teams that may be at different levels of research maturity or independence.
• Strong organizational skills, with the ability to manage multiple studies and priorities across different locations.
• Comfort working in roles similar to Clinical Research Manager or Research Program Manager within oncology.
• Interest in contributing to the growth and development of an expanding clinical research program.

This role is based within a cancer-focused research environment that includes a designated cancer institute setting with a robust clinical research infrastructure. The organization employs more than 200 professionals across a variety of specialties, including Clinical Research Coordinators, Regulatory Affairs staff, Clinical Research Managers, Nurse Managers, and research leadership. The Research Study Manager works as part of a multidisciplinary team dedicated to advancing oncology clinical trials, collaborating closely with physicians, site research staff, and central research administration. The environment emphasizes collaboration, regulatory compliance, and high-quality patient-centered research, offering opportunities to contribute to a growing oncology research program and to work with a broad range of clinical and operational experts.

This is a Contract to Hire position based out of New Brunswick, NJ.

The pay range for this position is $52.00 - $58.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a hybrid position in New Brunswick,NJ.

This position is anticipated to close on Sep 14, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

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Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.