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Entry Level Clinical Research Coordinator Jobs in Puerto Rico

Merck & Co.

Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready ... Good understanding and working knowledge of clinical research, phases of clinical trials, current ...

Merck & Co.

Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready ... Good understanding and working knowledge of clinical research, phases of clinical trials, current ...

Mount Sinai Medical Center

PR

... research. At Mount Sinai, we take pride in our achievements, aiming to be a beacon of quality ... clinical excellence. Position Responsibilities: * Administers & Coordinates medical prescribed ...

Deloitte

Epic Denials Management Operator

San Juan, PR · Remote

$17.75 - $23.50/hr

... clinical teams as needed. Provide additional documentation to payers as needed to resolve denial ... Document denial details, research conducted, and follow-up activities conducted in relevant EMR and ...

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Entry Level Clinical Research Coordinator information

What does an entry level clinical research coordinator do?

An entry-level clinical research coordinator (CRC) oversees clinical trials. Your duties as an entry-level coordinator depend on the type of research involved in the project and the needs of your employer; you may recruit patients for studies and coordinate with researchers to ensure they collect the right data during the trial and abide by all relevant regulations. An entry-level coordinator may focus on one aspect of the project, such as obtaining informed consent from participants or ensuring that data meets FDA requirements. As an entry-level employee, you work under senior project management staff who approve your plans or budgets before the trial begins.

What are the key skills and qualifications needed to thrive as an entry level clinical research coordinator, and why are they important?

To thrive as an Entry Level Clinical Research Coordinator, you need a bachelor’s degree in a health or science-related field, attention to detail, and a basic understanding of clinical research protocols. Familiarity with data management systems, regulatory documentation, and Good Clinical Practice (GCP) guidelines is often required. Strong organizational skills, effective communication, and the ability to work collaboratively help you excel in coordinating study activities and liaising with diverse stakeholders. These skills ensure accurate data collection, regulatory compliance, and smooth execution of clinical trials.

What are some common challenges faced by entry level clinical research coordinators, and how can they be addressed?

Entry-level Clinical Research Coordinators often face challenges such as quickly learning complex study protocols, managing multiple tasks simultaneously, and ensuring strict regulatory compliance. To address these challenges, it is helpful to develop strong organizational skills, seek mentorship from experienced colleagues, and stay up-to-date with Good Clinical Practice (GCP) guidelines. Regular communication with the research team and proactive problem-solving can also ease the transition into the role and contribute to successful study coordination.

What is the difference between Entry Level Clinical Research Coordinator vs Clinical Research Associate?

AspectEntry Level Clinical Research CoordinatorClinical Research Associate
Required CredentialsBachelor's degree, relevant certifications (e.g., CCRP)Bachelor's degree, often with additional certifications
Work EnvironmentResearch sites, hospitals, clinicsMonitoring sites, sponsor offices, CROs
Employer & Industry UsageHospitals, academic institutions, biotech companiesPharmaceutical companies, CROs, biotech firms
Common Search & ComparisonYesYes

While both roles involve clinical trial processes, Entry Level Clinical Research Coordinators typically manage trial activities at research sites, whereas Clinical Research Associates focus on monitoring and ensuring compliance across multiple sites. The roles often require similar educational backgrounds and certifications, but differ in daily responsibilities and work settings.

More about Entry Level Clinical Research Coordinator jobs

What are the most commonly searched types of Entry Level Clinical Research jobs in Puerto Rico?

The most popular types of Entry Level Clinical Research jobs in Puerto Rico are:

What job categories do people searching Entry Level Clinical Research Coordinator jobs in Puerto Rico look for?

The top searched job categories for Entry Level Clinical Research Coordinator jobs in Puerto Rico are:

Entry Level Clinical Research Coordinator jobs near you
Infographic showing various Entry Level Clinical Research Coordinator job openings in Puerto Rico 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.

Clinical Research Coordinator

Pan American Center for Oncology Trials LLC

San Juan, PR • On-site

$60 - $80/hr

Other

Posted 6 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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