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Clinical Research Operations Manager Jobs in Puerto Rico

Merck & Co.

... 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 ...

MSD

Sr. CRA - Clinical Research Associate

Guaynabo, PR · On-site

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

New

Merck & Co.

... 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 ...

Walgreens

Pharmacy Operations Manager

Dorado, 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 · 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

Guaynabo, 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 ...

DaVita

Healthcare Operations Manager

Vega Baja, PR · On-site

$94K - $148K/yr

Develop, mentor and inspire a cross-functional clinical team (census dependent on state laws) to ... Manage complete operation and performance of the clinic: adhere to budget, forecast expenses ...

IQVIA

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...

IQVIA, Inc.

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...

IQVIA

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...

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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 are popular job titles related to Clinical Research Operations Manager jobs in Puerto Rico?

For Clinical Research Operations Manager jobs in Puerto Rico, the most frequently searched job titles are:

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.

Clinical Research Coordinator

Pan American Center for Oncology Trials LLC

San Juan, PR • On-site

$55 - $75/hr

Other

Posted 5 days ago

Job description

We are seeking aClinical Research Coordinator to support the planning, execution, and management of clinical research studies. The ideal candidate will have strong experience in clinical research, solid knowledge of regulatory compliance, and the ability to work collaboratively with multidisciplinary teams to ensure high-quality study conduct and participant safety.

Responsibilities
  • Provide clear, professional, and compassionate communication to study participants, addressing questions and concerns throughout the study process.
  • Protect the well-being of research participants and ensure compliance with all regulatory guidelines, Good Clinical Practice (GCP), and study protocols.
  • Collaborate with investigators, epidemiologists, statistical consultants, research associates, regulatory staff, and other personnel to support clinical studies.
  • Prepare, submit, and maintain research reports and documentation according to protocols and institutional policies.
  • Coordinate the receipt, handling, dispensing, and administration of investigational products (medications, vaccines, or study agents).
  • Maintain communication with sponsors, study monitors, co-investigators, regulatory offices, and internal leadership.
  • Participate in research meetings and assist in coordinating sponsor-required and internal operational meetings.
  • Screen, recruit, and consent study participants according to protocol criteria and ethical standards.
  • Assist with medical evaluations, procedures, adverse event assessments, and other clinical tasks under the guidance of the Principal Investigator or physician scientist.
  • Review medical records and source documents to support clinical interventions, safety assessments, and data verification.
  • Collect, validate, and enter clinical data into study databases, ensuring accuracy and regulatory compliance.
  • Maintain organized and compliant research documentation for audit readiness.
Qualifications
  • Bachelor's degree in Nursing (RN) or Medical Laboratory Technology (Lab Tech). Candidates holding a Medical Doctor (MD) degree or currently pursuing an MD are also encouraged to apply.
  • Knowledge of clinical research operations, human subjects protection, and basic healthcare processes.
  • Familiarity with GCP, FDA regulations, ICH guidelines, and ethical standards in clinical research.
  • Ability to assist with basic clinical procedures and medical assessments within scope of training.
  • Excellent verbal and written communication skills in English and Spanish.
  • Strong organizational skills and ability to manage multiple studies and documentation.
  • High attention to detail, analytical thinking, and commitment to data integrity and participant safety.
  • Proficiency with EDC systems, EMR/EHR platforms, and Microsoft Office Suite.
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