1

Hiv Clinical Research Jobs (NOW HIRING)

Clinical Research Coordinator I

Boston, MA · On-site

$26.25 - $35/hr

As a not-for-profit, we support patient care, research, teaching, and community service, striving ... Assessing the clinical and economic outcomes from HIV prevention resource allocation in the US ...

Showing results 21-40

Hiv Clinical Research information

See salary details

$13

$24

$40

How much do hiv clinical research jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for hiv clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is HIV clinical research?

HIV clinical research involves scientific studies and trials focused on understanding, preventing, diagnosing, and treating HIV infection. These studies may test new medications, vaccines, or treatment approaches to improve patient outcomes and quality of life. Researchers also investigate ways to prevent transmission and manage complications associated with HIV. Clinical research is essential for developing safer, more effective therapies and ultimately working toward an HIV cure.

What are the key skills and qualifications needed to thrive in HIV clinical research, and why are they important?

To thrive in HIV Clinical Research, you need a strong foundation in medical or life sciences, experience in clinical trial protocols, and often an advanced degree such as an MD, RN, or PhD. Familiarity with clinical trial management systems, regulatory compliance (such as GCP), and data analysis software is typically required. Excellent communication, attention to detail, and organizational skills help researchers collaborate effectively and ensure ethical, accurate data collection. These competencies are crucial for maintaining research integrity, participant safety, and the advancement of HIV treatment options.

What are some common challenges faced by professionals working in HIV clinical research, and how are they addressed?

Professionals in HIV clinical research often encounter challenges such as recruiting and retaining study participants, navigating complex regulatory requirements, and managing sensitive patient data. To address these, teams typically employ community outreach strategies to build trust with potential participants, maintain continuous training on ethical and regulatory standards, and utilize secure electronic systems for data management. Collaboration with multidisciplinary teams—including clinicians, data managers, and community liaisons—is essential for overcoming these obstacles and ensuring the success of research studies.

What is the difference between Hiv Clinical Research vs Hiv Clinical Trial Coordinator?

AspectHiv Clinical ResearchHiv Clinical Trial Coordinator
CredentialsTypically requires a background in healthcare, nursing, or life sciences; certifications like CCRP or CCRC are commonOften requires similar healthcare or research certifications; experience in trial coordination is preferred
Work EnvironmentResearch institutions, hospitals, or pharmaceutical companies conducting HIV studiesClinical trial sites, hospitals, or research centers managing trial logistics
Employer & IndustryResearch organizations, biotech firms, academic institutionsClinical research sites, hospitals, pharmaceutical companies

Hiv Clinical Research involves designing, managing, and analyzing HIV studies, often requiring advanced research skills. In contrast, Hiv Clinical Trial Coordinators focus on the day-to-day operations of clinical trials, ensuring protocol adherence and participant management. Both roles are vital in advancing HIV treatment but differ in scope and responsibilities.

More about Hiv Clinical Research jobs

What cities are hiring for Hiv Clinical Research jobs?

Cities with the most Hiv Clinical Research job openings:

What states have the most Hiv Clinical Research jobs?

States with the most job openings for Hiv Clinical Research jobs include:

What job categories do people searching Hiv Clinical Research jobs look for?

The top searched job categories for Hiv Clinical Research jobs are:

Infographic showing various Hiv Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

$27.50 - $36.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago


Job description

Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.

With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world’s leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world’s deadliest diseases and make life beyond cancer a reality.

At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.

At Fred Hutchinson Cancer Center, all employees are expected to demonstrate a commitment to our values of collaboration, compassion, determination, excellence, innovation, integrity, and respect.

The Clinical Research Coordinator II is responsible for day-to-day coordination of interventional Phase I-III clinical trials and observational Cancer Control studies. The position will oversee all subject-level study workflows including screening patients for eligibility, performing enrollments, tracking patient visits, abstracting and reporting study data, coordinating research specimen collection and submission, and creating and maintaining research documentation. Collaborates with Data Coordination staff on the Clinical Research Support team.

Reporting to the Research Manger of Clinical Trials Coordination, the coordinator will be part of specialized Oncology research teams, including Nuclear Medicine and Neurology. This position is key to the smooth operation of clinical trials and advancing research efforts at Fred Hutch. 

This role works with Nuclear Medicine Trials that involve radiopharmacuticals. 


  • Conduct daily clinical operations of assigned research studies in accordance with study protocols, GCP guidelines, applicable regulatory requirements and institutional policies. 
  • Coordinate patient enrollment and participation by reviewing study candidates’ medical records for eligibility, initiating enrollment, ensuring informed consent, and maintaining accurate enrollment records.  
  • Schedule patient clinic visits and on-going study visits; ensure compliance with study protocols with respect to clinical procedures, laboratory tests and other patient activities; may administer study questionnaires and ensure drug self-administration accountability with patients. 
  • Complete clinical requisition forms as instructed, assemble kits for patient visits, transport laboratory samples and ensure samples are processed and shipped according to study guidelines; track and maintain research supplies. 
  • Identify, track and confirm billable activities for patients; work with internal finance team to assist in reviewing clinic charges to ensure billing compliance. 
  • Act as protocol liaison with clinical teams, patients, and providers on study related topics. 
  • Prepare and coordinate monitoring visits and respond to queries and other requests from study monitors, following up with and resolving any issues that may arise. 
  • Assist with maintaining appropriate source documentation and/or performing case report form (CRF) data entry. 
  • Will travel from South Lake Union campus on shuttle to UW Medical Center (UWMC) Montlake to coordinate patient visits and collection of research specimens for processing and shipping.
  • Other duties as assigned.

MINIMUM QUALIFICATIONS:

  • High school diploma or equivalent.
  • Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
  • Knowledge of clinical trials records, procedures, and computerized data processing systems.
  • Demonstrated knowledge of how to synthesize study conduct.

PREFERRED QUALIFICATIONS:

  • Associate or bachelor’s degree preferred.
  • Certified Clinical Research Coordinator (CCRC) or certification as Clinical Research Professional (SOCRA).
  • Minimum five years of experience in a research environment with regulatory or human research protections.
  • Previous experience working with NIH, FDA and OHRP regulations and medical terminology.
  • Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
  • Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
  • Ability to work with multiple data management systems including generating reports and sourcing data from systems.
  • Ability to extract data from medical records.
  • Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to escalate questions and concerns when appropriate.

The hourly pay range for this position is from $31.83 to $47.73 and pay offered will be based on experience and qualifications.
Although Fred Hutch is not sponsoring most H-1B visas at this time, candidates who already hold an H-1B sponsored by another organization and are currently in the U.S. may be eligible for this position.
Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (12-22 days per year), paid sick leave (12-25 days per year), paid holidays (13 days per year), and paid parental leave (up to 4 weeks).


We are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to Human Resources at hrops@fredhutch.org or by calling 206-667-4700.