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Lab Coordinator Jobs in Puerto Rico (NOW HIRING)

Johnson & Johnson

QC Incoming Coordinator

Gurabo, PR · On-site

$19 - $26.25/hr

Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... The Coordinator must ensure compliance with all quality control policies, procedures, and systems ...

Fresenius Medical Care

Union Dietitian

San German, PR · On-site

... lab parameters pertaining to their disease process. * Completes nutritional assessment and ... Collaborates and coordinates with team members in provision of Pre-ESRD education as appropriate.

Fresenius Medical Care

Union Dietitian

Mayaguez, PR · On-site

... lab parameters pertaining to their disease process. * Completes nutritional assessment and ... Collaborates and coordinates with team members in provision of Pre-ESRD education as appropriate.

Eaton

PLS Manager

Las Piedras, PR · On-site

Coordinates project activities with other operating or engineering units to facilitate ... Manage MET Lab daily accountability as well as capital expending for Lab projects. * Support plant ...

Eaton Corporation

PLS Manager

Las Piedras, PR · On-site

$100 - $125/hr

Coordinates project activities with other operating or engineering units to facilitate ... Manage MET Lab daily accountability as well as capital expending for Lab projects. * Support plant ...

New

Eaton

PLS Manager

Las Piedras, PR

Coordinates project activities with other operating or engineering units to facilitate ... Manage MET Lab daily accountability as well as capital expending for Lab projects. * Support plant ...

DaVita

Patient Care Technician

Fort Buchanan, PR

$13.50 - $17.75/hr

This role provides hands-on support, education, and care coordination under RN supervision to ... Monitor vital signs and collect lab specimens as needed * Maintain equipment and ensure compliance ...

JC Automation

Equipment Manager

Carolina, PR · On-site

$150 - $200/hr

Lead SAT planning and execution coordination with C&Q and the System Turnover Lead. * Manage vendor ... Non-discipline-specific major equipment and vendor packages -- process and utility skids, lab ...

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Lab Coordinator information

What is a lab coordinator?

A lab coordinator manages the operations of a science laboratory. As a lab coordinator, your primary job duties include coordinating lab use, acquiring new materials, maintaining equipment, and ensuring all safety rules and regulations are met. The career may also involve working with hazardous materials, such as body fluids or disease organisms. To become a lab coordinator, you must have at least a bachelor’s degree, usually in a scientific field, as well as experience using lab tools and equipment. Additional qualifications include excellent analytical, communication, and managerial skills.

What are some common challenges faced by lab coordinators, and how can they be addressed?

Lab Coordinators often juggle multiple responsibilities, such as managing inventory, ensuring equipment maintenance, and coordinating with researchers or students. One common challenge is balancing administrative tasks with hands-on support, especially during busy periods or when resources are limited. Effective time management, clear communication, and establishing standardized procedures can help overcome these challenges. Building strong relationships with faculty, technicians, and suppliers also streamlines workflows and minimizes disruptions.

What are the key skills and qualifications needed to thrive as a lab coordinator, and why are they important?

To thrive as a Lab Coordinator, you need strong organizational skills, laboratory safety knowledge, and a relevant science degree or experience in lab management. Familiarity with laboratory information management systems (LIMS), lab equipment, and safety certifications like OSHA training are typically required. Excellent communication, attention to detail, and problem-solving abilities help you manage workflows and coordinate between researchers, staff, and students. These skills ensure safe, efficient, and accurate laboratory operations that support research and educational objectives.

What is the difference between Lab Coordinator vs Lab Technician?

AspectLab CoordinatorLab Technician
Required CredentialsTypically a bachelor's degree in a science or related fieldUsually an associate degree or certification in a specific lab area
Work EnvironmentOversees lab operations, manages schedules, and coordinates activitiesPerforms hands-on testing, sample preparation, and data collection
Employer & Industry UsageUsed in research labs, healthcare, and industrial settings for management rolesCommon in clinical, research, and manufacturing labs for technical tasks

While both roles work within laboratory settings, the Lab Coordinator primarily manages lab operations and staff, whereas the Lab Technician focuses on performing technical testing and data collection. Understanding these differences helps in choosing the right career path or job search focus.

More about Lab Coordinator jobs

What are the most commonly searched types of Lab jobs in Puerto Rico?

The most popular types of Lab jobs in Puerto Rico are:

What are popular job titles related to Lab Coordinator jobs in Puerto Rico?

For Lab Coordinator jobs in Puerto Rico, the most frequently searched job titles are:

Lab Coordinator jobs near you
Infographic showing various Lab Coordinator job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution.

Clinical Research Coordinator

Pan American Center for Oncology Trials LLC

San Juan, PR • On-site

$60 - $80/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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