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How much do full time obesity research jobs pay per year?

As of Sep 6, 2026, the average yearly pay for full time obesity research in the United States is $99,840.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $115,500.00 per year, depending on experience, location, and employer.

What is a full time obesity researcher?

A Full Time Obesity Researcher is a professional who dedicates their career to studying the causes, effects, prevention, and treatment of obesity. They may work in academic, clinical, governmental, or private settings, conducting experiments, analyzing data, and publishing findings. Their research often helps inform public health policies and clinical guidelines for managing obesity. These researchers usually have backgrounds in fields like medicine, nutrition, epidemiology, or public health. Their work is critical in addressing the global obesity epidemic and improving overall health outcomes.

What are the key skills and qualifications needed to thrive as a full time obesity researcher?

To thrive as a Full Time Obesity Researcher, you need a solid background in biomedical sciences, epidemiology, or nutrition, often supported by a relevant graduate degree such as an MSc or PhD. Familiarity with statistical software (e.g., SPSS, R, SAS), clinical trial protocols, and research ethics certifications is typically required. Strong analytical thinking, attention to detail, and effective communication skills distinguish top candidates in this field. These competencies are crucial for conducting rigorous research, securing funding, and translating findings into impactful health interventions.

What are some common challenges faced by professionals working in full time obesity research, and how can they be managed?

Professionals in full-time obesity research often encounter challenges such as recruiting and retaining study participants, managing large and complex datasets, and staying updated with evolving methodologies. Ethical considerations and maintaining participant confidentiality are also critical. Collaborating closely with interdisciplinary teams, including clinicians, statisticians, and behavioral scientists, helps address these challenges and fosters innovative solutions. Regular training and attending relevant conferences can further support professional growth and effective problem-solving in this dynamic field.
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Full Time Obesity Research jobs near you
Infographic showing various Full Time Obesity Research job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $99,840 per year, or $48 per hour.

Physician, MD/DO - Clinical Research

Headlands Research

San Juan, PR • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 25 days ago

Key responsibilities

  • Lead and oversee clinical trials at the site, ensuring compliance with protocols, regulatory standards, and ethical guidelines.

  • Provide leadership, mentorship, and training to research staff to support high-quality study execution.

  • Obtain IRB approval for study initiation and protocol modifications, and communicate with stakeholders including sponsors, monitors, and regulators.

Job description

 Location: San Juan, PR  | Site Name: CMR Center  | Full-Time  | Clinical Research

We're seeking an experienced physician for our clinical research site located in San Juan, PR to serve as our Principal Investigator on clinical trials. The Principal Investigator is responsible for ensuring subject safety, protocol compliance, data integrity, and high-quality study execution in accordance with FDA regulations, ICH-GCP guidelines, sponsor requirements, and company standards. 

This role is ideal for a physician who is interested in clinical research, passionate about improving patient access to innovative therapies, and helping expand research opportunities in the community. In addition to clinical and study oversight responsibilities, the Principal Investigator will support business development and community engagement efforts, including attending sponsor meetings, conducting physician outreach, attending community education events, engaging in media interviews, and others that help build awareness of clinical research. 

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:00am - 5:00pm
Location:  Onsite in San Juan, PR (no capabilities for remote or hybrid work)
Reports to:  Site President
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

The Company

CMRC Headlands is a premier clinical research site conducting Phase II-IV clinical trials in collaboration with global pharmaceutical sponsors. We advance medical innovation while placing patient experience and operational excellence at the heart of our mission. 

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do. 

Responsibilities:

  • Lead and oversee clinical trials conducted at CMR Center, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
  • Eligible for or active unencumbered license to practice as an MD or DO in Puerto Rico required.
  • Must be board-certified or board-eligible.
  • Bilingual in English and Spanish required
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.
  • Experience in obesity, cardiometabolic disease, vaccines, CNS, gastroenterology, rheumatology, nephrology, pediatrics, or other relevant therapeutic areas preferred.
  • Existing patient access, referral network, or community relationships preferred. 

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