ZipRecruiter

Log In

1

Clinical Research Operations Manager Jobs in Puerto Rico

Headlands Research

Clinical Research Nurse, RN

San Juan, PR

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Clinical Research Manager Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts ...

Headlands Research

Clinical Research Nurse, RN

San Juan, PR · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Clinical Research Manager Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts ...

Headlands Research

Medical Assistant, Research Assistant

San Juan, PR · On-site

$17.50 - $22.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and general clinical research operations. This position requires strong organization ... Enter and verify study data in Electronic Data Capture systems, Clinical Trial Management Systems ...

Merck & Co.

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... CRM, TA Head and CRD as needed.Works in partnership with GCTO country operations, finance ... Good understanding and working knowledge of clinical research, phases of clinical trials, current ...

Merck & Co.

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... CRM, TA Head and CRD as needed.Works in partnership with GCTO country operations, finance ... Good understanding and working knowledge of clinical research, phases of clinical trials, current ...

Merck & Co.

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... CRM, TA Head and CRD as needed.Works in partnership with GCTO country operations, finance ... Good understanding and working knowledge of clinical research, phases of clinical trials, current ...

New

Walgreens

PR · On-site

* Where state and federal laws/regulations allow, accountable for performing day-to-day non-clinical ... Manages core pharmacy workflow and drives excellence in pharmacy operations. Coordinates and ...

Walgreens

PR · On-site

* Where state and federal laws/regulations allow, accountable for performing day-to-day non-clinical ... Manages core pharmacy workflow and drives excellence in pharmacy operations. Coordinates and ...

Walgreens

Pharmacy Operations Manager

Carolina, PR

* Where state and federal laws/regulations allow, accountable for performing day-to-day non-clinical ... Manages core pharmacy workflow and drives excellence in pharmacy operations. Coordinates and ...

next page

Showing results 1-20

All JobsClinical Research Operations JobsClinical Research Operations Manager JobsClinical Research Operations Manager Jobs in Puerto Rico

Clinical Research Operations Manager information

What does a clinical research operations manager do?

A Clinical Research Operations Manager oversees the daily operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate between research staff, sponsors, and regulatory bodies, manage budgets and timelines, and ensure proper documentation and reporting. Their role is essential in maintaining the quality and integrity of clinical studies from start to finish.

How does a clinical research operations manager collaborate with cross-functional teams during a study?

As a Clinical Research Operations Manager, you will work closely with cross-functional teams including clinical trial coordinators, data managers, regulatory affairs specialists, and principal investigators. Your role involves facilitating clear communication between departments, ensuring that study milestones are met, and resolving operational issues as they arise. Regular meetings and status updates are common, and you'll often act as a liaison to keep all stakeholders aligned on study objectives, timelines, and compliance requirements. This collaborative approach is crucial for maintaining study integrity and ensuring successful trial outcomes.

What are the key skills and qualifications needed to thrive as a clinical research operations manager, and why are they important?

To thrive as a Clinical Research Operations Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valuable. Leadership, problem-solving, and excellent organizational and communication skills help you manage teams and collaborate effectively with stakeholders. These skills and qualities are crucial for ensuring the successful execution of clinical trials while maintaining regulatory standards and operational efficiency.

What job categories do people searching Clinical Research Operations Manager jobs in Puerto Rico look for?

The top searched job categories for Clinical Research Operations Manager jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Clinical Research Operations Manager jobs?

Cities in Puerto Rico with the most Clinical Research Operations Manager job openings:

Clinical Research Operations Manager jobs near you
Infographic showing various Clinical Research Operations Manager job openings in Puerto Rico as of August 2026, with employment types broken down into 84% Full Time, 12% Part Time, 2% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Physician, MD/DO - Clinical Research

Headlands Research

San Juan, PR

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 4 days ago

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. 

Apply