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Senior Clinical Research Associate Jobs in Puerto Rico

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 Research Associate (CRA) based in Puerto Rico to join our team and play a key role in delivering high ...

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 Research Associate (CRA) based in Puerto Rico to join our team and play a key role in delivering high ...

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 Research Associate (CRA) based in Puerto Rico to join our team and play a key role in delivering high ...

Merck & Co.

Actively develops and expands the territory for clinical research, finding and developing new sites ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Merck & Co.

Actively develops and expands the territory for clinical research, finding and developing new sites ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

DaVita

Director of Clinical Services (RN)

San Juan, PR · On-site

$78K - $106K/yr

Director of Clinical Services The Director of Clinical Services (DCS) serves as the senior clinical ... Associate Degree in Nursing (ASN) or Bachelor's Degree in Nursing (BSN) or related field. * Minimum ...

Organon

Medical Science Liaison - Florida

Florida, PR · On-site

Clear understanding of clinical research methodologies and ability to independently evaluate and ... Senior Stakeholders Who We Are: Organon delivers ingenious health solutions that enable people to ...

Organon

Medical Science Liaison - Florida

Florida, PR · On-site

Clear understanding of clinical research methodologies and ability to independently evaluate and ... Senior Stakeholders Who We Are: Organon delivers ingenious health solutions that enable people to ...

Kelly Services

Sr Associate QA

Juncos, PR · On-site

How about this one? We're seeking for a Sr Associate QA to work in the east region, in PR. With us ... Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to ...

PenFed Credit Union

PR · On-site

Research programs and processes to fully understand affected processes, determine problem cause and ... Present to senior/assigned technical staff for review and guidance on testing, verification of ...

Biopharma-Consulting-Jad-Group

Sr. Engineer

Juncos, PR · On-site

$110 - $170/hr

Supervise, coordinate, and review the work of engineers, associates, and technicians on both ... Collaborate with manufacturing, research, process development, utilities, facilities, quality ...

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All JobsClinical Research Associate JobsSenior Clinical Research Associate JobsSenior Clinical Research Associate Jobs in Puerto Rico

Senior Clinical Research Associate information

What does a senior clinical research associate do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

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

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What are some typical challenges faced by senior clinical research associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.
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Senior Clinical Research Associate jobs near you

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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