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Clinical Research Program Manager Jobs in Puerto Rico

Merck & Co.

Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.Actively develops and expands the territory for ...

Merck & Co.

Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.Actively develops and expands the territory for ...

Merck & Co.

Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.Actively develops and expands the territory for ...

New

US Department of the Treasury

Program Manager

Caguas, PR · On-site

$125K/yr

Specialized experience would include one year of substantive supervisory or program management ... Experience conducting operational research by evaluating program data, identifying organizational ...

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Clinical Research Program Manager information

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

What are the key skills and qualifications needed to thrive as a clinical research program manager?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What is the difference between Clinical Research Program Manager vs Clinical Research Coordinator?

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

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

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

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

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

Clinical Research Program Manager jobs near you

Clinical Research Nurse, RN

Headlands Research

San Juan, PR

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago

Job description

Clinical Research Nurse (RN)

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

Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.

We're seeking a Clinical Research Nurse (RN) for our clinical research site located in San Juan, PR. The ideal candidate has a background in hospital or private clinical practice, is passionate about patient-centered care, and thrives in a fast-paced, ambiguous, research-driven environment. This role requires a proactive self-starter who can navigate complex protocols with clinical judgment, independence, and attention to detail. Bilingual fluency in English and Spanish is essential.

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:30am - 4:30pm
Location:  Onsite in San Juan, PR (no capabilities for remote or hybrid work)
Reports to:  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 (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

  What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission-driven culture focused on advancing medicine and improving patient outcomes
 Why Join Us?

You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.

Responsibilities:

  • Perform and document pediatric and adult phlebotomy procedures
  • Administer and document vital signs and clinical assessments
  • Support all phases of patient interaction including screening, enrollment, dosing, and follow-ups
  • Act as clinical support during study visits-monitor, document, and report on patient status and adverse events
  • Manage specimen handling, labeling, storage, and timely shipment according to protocol
  • Provide clinical oversight for study-related procedures to ensure safety and compliance
  • Coordinate and schedule research visits and procedures with precision and patient sensitivity
  • Review and interpret study protocols through a clinical lens to anticipate patient care needs
  • Communicate effectively with investigators, monitors, sponsors, and internal teams
  • Support study recruitment and patient outreach strategies
  • Maintain and organize source documentation and regulatory binders
  • Prepare for monitoring visits and assist during sponsor or regulatory audits
  • Other duties as needed to support study execution

Requirements:

  • Fluent in English and Spanish (written and verbal) required
  • Current and unencumbered license to practice as a Registered Nurse in Puerto Rico required
  • Minimum of 6 years of experience in a clinical setting (hospital or private practice) required
  • Minimum of 4 years drawing blood from both pediatric and adult patients required
  • Solid understanding of Good Clinical Practice (GCP) and/or willingness to undergo training
  • Comfort working within protocol-driven environments with shifting timelines
  • Demonstrated ability to operate autonomously and take initiative within a small, agile team
  • Proficient with electronic medical records, clinical data entry, and laboratory documentation
  • Exceptional organizational and multitasking skills
  • Strong interpersonal skills and compassionate bedside manner
  • Prior experience in clinical research or investigational trials is a plus
  • Familiarity with FDA, ICH-GCP, and HIPAA compliance standards a plus
  • Experience preparing for and interacting with clinical trial monitors a plus

Apply