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Study Director Jobs in Virginia (NOW HIRING)

Louisiana State University

$42K - $51K/yr

Identifies special projects and partners with the Director of Study Abroad to further the goals of the Study Abroad Office. Professional Development (10%) * Ensures program quality and continual self ...

LSU AgCenter

$42K - $51K/yr

Identifies special projects and partners with the Director of Study Abroad to further the goals of the Study Abroad Office. Professional Development (10%) * Ensures program quality and continual self ...

Louisiana Workforce Commission

$42K - $51K/yr

Identifies special projects and partners with the Director of Study Abroad to further the goals of the Study Abroad Office. Professional Development (10%) * Ensures program quality and continual self ...

SoBran, Inc.

Veterinary Technician I-VA

Norfolk, VA · On-site

$20 - $30/hr

Assists veterinarian, PI or Study Director with surgical procedures. * Collects, preserves and prepares any biological samples such as; tissue, blood, urine, fecal samples and/or skin scrapings.

SoBran Inc.

Veterinary Technician I-VA

Norfolk, VA · On-site

$20 - $30/hr

Assists veterinarian, PI or Study Director with surgical procedures. * Collects, preserves and prepares any biological samples such as; tissue, blood, urine, fecal samples and/or skin scrapings.

Liberty

Event Officer - Work Study

Lynchburg, VA

$12.77/hr

Work Study Direct Customers * On site coordinator and facility managers * Coordinate with resource team while onsite QUALIFICATIONS AND CREDENTIALS Education and Experience Working toward a four-year ...

Liberty

Event Officer - Work Study

Lynchburg, VA · On-site

$12.77/hr

Work Study Direct Customers * On site coordinator and facility managers * Coordinate with resource team while onsite QUALIFICATIONS AND CREDENTIALS Education and Experience Working toward a four-year ...

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Study Director information

See Virginia salary details

$44.6K

$127.3K

$230.5K

How much do study director jobs pay per year?

As of Aug 25, 2026, the average yearly pay for study director in Virginia is $127,266.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $186,900.00 per year, depending on experience, location, and employer.

What is a study director?

A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.

What does a study director do?

As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

How does a study director typically collaborate with cross-functional teams during a research project?

As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.

What skills and qualifications does a successful study director have?

To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.

What is the difference between Study Director vs Laboratory Manager?

AspectStudy DirectorLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and relevant certificationsRequires relevant degrees and management experience, but not necessarily advanced research credentials
Work EnvironmentLeads specific research or regulatory studies, often in contract labs or pharmaceutical companiesOversees daily lab operations, staff, and compliance across multiple projects
Industry UsageCommonly used in GLP, clinical, and research settingsUsed broadly in laboratory settings across industries

The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.

More about Study Director jobs

What are the most commonly searched types of Study jobs in Virginia?

The most popular types of Study jobs in Virginia are:

What are popular job titles related to Study Director jobs in Virginia?

For Study Director jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Study Director jobs in Virginia look for?

The top searched job categories for Study Director jobs in Virginia are:

What cities in Virginia are hiring for Study Director jobs?

Cities in Virginia with the most Study Director job openings:

Study Director jobs near you
Infographic showing various Study Director job openings in Virginia as of August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $127,266 per year, or $61.2 per hour.

Director, Nursing & Study Operations

The START Center for Cancer Research

Virginia Beach, VA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

The START Center for Cancer Research ("START") is the world's largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access"tocutting edgetrials throughout the UnitedStatesand Europe.
The START Center for Cancer Research is seeking a Director of Nursing & Study Operations. The Director of Nursing & Study Operations is a dual-function leadership role responsible for the oversight and performance of START's nursing teams and clinical research operations. This role ensures compliant, efficient, and high-quality care and study conduct across departments, while supporting START's goals for study growth, operational excellence, and patient care. The Director leads Clinical Research Coordinators, Medical Records, Data Coordinators, Clinic Nurses, Infusion Nurses, Nurse Navigators, Referral Intake and Scheduling teams. The position works collaboratively across departments including Quality, Regulatory, Finance, and Site Development.
Site: START Norfolk
Work Schedule: Monday-Friday 8:00am-5:00pm
Essential Responsibilities
Leadership & Oversight
  • Provide effective, proactive leadership to Clinical Research Coordinators, Data Coordinators, Medical Records staff, Clinic Nurses, Infusion Nurses, Nurse Navigators, Referral Intake and Schedulers.
  • Provide training, coaching, and development for direct reports, ensuring ongoing competency and alignment with START's values and expectations.
  • Promote high-quality, patient-centered care and research delivery across clinical and study workflows.

Operational Management
  • Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility.
  • Supervise implementation of CTMS, EHR, and other clinical documentation systems.
  • Ensure accurate and timely data capture, monitor engagement, and audit preparedness across departments.
  • Oversee use of effective workflows and SOPs; lead ongoing review and revision efforts.

Clinical & Study Collaboration
  • Serve as clinical and operational liaison to investigators, quality team, regulatory, pharmacy, and global shared services.
  • Partner with leaders to ensure compliant delivery of care within the scope of research protocols.
  • Support review and feasibility assessment of new protocols with attention to nursing and operational capacity.
  • Ensure equitable study allocation and ongoing support for study teams.

Process Improvement & Strategic Support
  • Use continuous improvement techniques to streamline workflows and resolve care or operational bottlenecks.
  • Track key metrics across referrals, screening, enrollment, and patient satisfaction.
  • Participate in strategic initiatives and regional projects to expand access and improve operational performance.
  • Collaborate with quality and compliance teams to uphold all applicable federal, GCP, and GDPR regulations.
  • Other duties may be assigned at any time.

Required Education and Experience:
  • Bachelor's degree in Nursing or Health-related field
  • RN license in good standing with state
  • Minimum 5 years of leadership experience in oncology clinical research
  • CITI GCP training
  • Strong working knowledge of federal clinical research regulations, GCP, and GDPR
  • Familiarity with Microsoft Office applications and EHR/CTMS systems

Preferred Education and Experience:
  • Advanced degree (MSN, MHA, MBA, or related)
  • ONS/ONCC chemotherapy immunotherapy certificate
  • Oncology Certified Nurse (OCN)

Physical & Travel Requirements:
  • Approximately 80% of time is spent sitting
  • Very fast-paced and ever-changing healthcare environment
  • Demanding deadlines and constant knowledge updates required
  • Works closely with physicians and cross-functional teams
  • Intermittent travel to support site activation and training (<10%)

Best-in-Class Benefits and Perks
We value our employees' time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
  • Comprehensive health coverage: Medical, dental, and vision insurance provided
  • Robust retirement planning: 401(k) plan available with employer matching
  • Financial security: Life and disability insurance for added protection
  • Flexible financial options: Health savings and flexible spending accounts offered
  • Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
  • Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world's largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world.
Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

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