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Clinical Laboratory Technologist Jobs in Puerto Rico

Mount Sinai Medical Center

PR · On-site

In delivering an unmatched level of clinical expertise, our medical center is committed to ... Follow laboratory policy in regards to standard precautions, wearing of PPE, disposal of ...

Kelly Services

PQA Analyst

Barceloneta, PR · On-site

At Kelly ® Science, Engineering, Technology & Telecom (SETT) , we're passionate about helping you ... Ensure investigations of TPM plant events related but not limited to process, laboratory, raw ...

Mbc-Talent-Connections

Veterinary Surgeon

Carolina, PR · On-site

$120 - $170/hr

... technology * Comprehensive in-house laboratory and instrumentation supporting advanced orthopedic ... Collaborative team including specialists and emergency clinicians delivering comprehensive care ...

Pinnaql

Specialist QA (5:00 pm - 5:30 am)

Juncos, PR · On-site

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug ...

Kelly Services

Microbiologist

Carolina, PR · On-site

... Technology, Natural Sciences, Chemistry, or Biology * Two years or more of laboratory or related ... Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to ...

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Clinical Laboratory Technologist information

What is a clinical laboratory technologist?

Clinical Laboratory Technologists are healthcare professionals who perform complex tests on blood, bodily fluids, and tissue samples to help diagnose, treat, and prevent diseases. They operate sophisticated laboratory equipment, analyze results, and ensure the accuracy and reliability of test data. Their work is essential in supporting doctors and other healthcare providers in making informed medical decisions. Clinical Laboratory Technologists often specialize in areas such as microbiology, hematology, or immunology.

What are the key skills and qualifications needed to thrive as a clinical laboratory technologist?

To thrive as a Clinical Laboratory Technologist, you need a solid background in biology, chemistry, and laboratory procedures, typically supported by a bachelor's degree in medical technology or a related field and professional certification (such as ASCP). Familiarity with laboratory information systems (LIS), automated analyzers, and quality control protocols is essential. Attention to detail, critical thinking, and strong communication skills help technologists accurately process samples and collaborate with medical staff. These skills and qualities are crucial for ensuring reliable test results, patient safety, and the effective functioning of healthcare teams.

What are some common challenges clinical laboratory technologists face in maintaining accuracy and efficiency under time constraints?

Clinical Laboratory Technologists often work in fast-paced environments where timely and accurate results are critical for patient care. Balancing high sample volumes, strict quality control protocols, and complex instrumentation can be challenging, especially during peak periods or emergencies. Effective organization, attention to detail, and clear communication with healthcare teams are essential to overcome these challenges and minimize errors. Many laboratories also support continuing education and mentorship to help technologists stay current with advancements and improve workflow efficiency.

What is the difference between Clinical Laboratory Technologist vs Medical Laboratory Technician?

AspectClinical Laboratory TechnologistMedical Laboratory Technician
CredentialsBachelor's degree in medical technology or related field, certification often requiredAssociate's degree in medical laboratory technology, certification preferred
Work EnvironmentHospitals, diagnostic labs, research facilitiesSimilar settings, often working under supervision of technologists
Job ResponsibilitiesPerform complex tests, analyze results, validate dataPrepare samples, perform routine tests, assist technologists

The main difference between a Clinical Laboratory Technologist and a Medical Laboratory Technician lies in their education, responsibilities, and level of independence. Technologists typically hold a bachelor's degree and perform more complex testing and analysis, while technicians usually have an associate's degree and handle routine tasks under supervision. Both roles are essential in laboratory operations and often work together to ensure accurate diagnostic results.

How many years does it take to be a clinical laboratory technologist?

Becoming a clinical laboratory technologist typically requires completing a bachelor's degree in medical laboratory science or a related field, which generally takes about four years. Some positions may require certification or licensing, which can involve additional training or exams after graduation.

What are popular job titles related to Clinical Laboratory Technologist jobs in Puerto Rico?

For Clinical Laboratory Technologist jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Clinical Laboratory Technologist jobs in Puerto Rico look for?

The top searched job categories for Clinical Laboratory Technologist jobs in Puerto Rico are:

What are popular job titles related to Clinical Laboratory Technologist jobs in PR?

For Clinical Laboratory Technologist jobs in PR, the most frequently searched job titles are:

Clinical Laboratory Technologist jobs near you
Infographic showing various Clinical Laboratory Technologist job openings in Puerto Rico as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person 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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