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Clinical Research Project Assistant Jobs in Puerto Rico

Alcanza

Transport Driver

San Juan, PR

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations ... Participate in required trainings and meetings * Assist with other projects or tasks assigned or ...

FITS LLC

Project Manager

Manati, PR · On-site

Oversee and assist Engineers with their assigned projects. * Support the execution activities of ... Collaborate extensively with research, manufacturing, maintenance, process development, utilities ...

FITS LLC

Project Manager

Cayey, PR · On-site

... * Assist in technical, financial, and organizational issues by researching issues, providing recommendations and maintaining document archives. * Maintain and track project budget(s). * Reconcile ...

Organon

Medical Science Liaison

San Juan, PR · On-site

... * Assist in the scientific training for Commercial and other internal colleagues regarding ... Clear understanding of clinical research methodologies and ability to independently evaluate and ...

STI

Administrative Assistant

San Juan, PR · On-site

$17.75 - $23.75/hr

... Assist with research, planning, and coordination of team events • Assist with planning and ... agencies PMO activities: • Enter/review team members' expense reports Other: Assist with ...

STI

Administrative Assistant

San Juan, PR · On-site

$17.75 - $23.75/hr

... Assist with research, planning, and coordination of team events • Assist with planning and ... agencies PMO activities: • Enter/review team members' expense reports Other: Assist with ...

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All JobsClinical Research Project JobsClinical Research Project Assistant JobsClinical Research Project Assistant Jobs in Puerto Rico

Clinical Research Project Assistant information

What do clinical research assistants do?

Clinical research assistants support the conduct of clinical trials by preparing study materials, recruiting and screening participants, collecting and managing data, and ensuring compliance with protocols and regulations. They often work under the supervision of investigators and may use electronic data capture tools or databases as part of their responsibilities.

What is the difference between Clinical Research Project Assistant vs Clinical Research Coordinator?

AspectClinical Research Project AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCR are common
Work EnvironmentSupports research teams in clinical settings, hospitals, or research institutionsManages daily clinical trial activities, interacts directly with patients and investigators
Employer & Industry UsageUsed by research institutions, hospitals, pharmaceutical companiesCommonly employed in clinical trial sites, hospitals, and research organizations

The Clinical Research Project Assistant primarily supports research activities and data management, while the Clinical Research Coordinator oversees trial operations and patient interactions. Both roles require similar educational backgrounds and certifications, but their responsibilities differ in scope and daily tasks.

How much money do clinical research assistants make?

Clinical research assistants typically earn a median annual salary of around $45,000 to $55,000, depending on experience, location, and the complexity of the research environment. Entry-level positions may start lower, while those with specialized skills or certifications can earn higher wages.

What does a research project assistant do?

A research project assistant supports the planning, coordination, and execution of clinical research studies. They handle tasks such as data collection, maintaining study documentation, scheduling participant visits, and ensuring compliance with protocols and regulations. Strong organizational skills and familiarity with research tools like electronic data capture systems are often required.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, such as a background in healthcare or life sciences, and often involves monitoring clinical trials. Entry-level roles in clinical research may include Clinical Trial Assistant or Research Coordinator, with CRAs generally needing several years of related experience or specialized training. Certifications like SOCRA or ACRP can also be beneficial for advancing to CRA roles.
What job categories do people searching Clinical Research Project Assistant jobs in Puerto Rico look for? The top searched job categories for Clinical Research Project Assistant jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Clinical Research Project Assistant jobs? Cities in Puerto Rico with the most Clinical Research Project Assistant job openings:
Clinical Research Project Assistant jobs near you
Physician, MD/DO - Clinical Research

Physician, MD/DO - Clinical Research

Headlands Research

San Juan, PR

Other

Medical, Dental, Vision, Life, PTO

Posted 14 days ago

Job description

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

We're seeking an experienced physician for our clinical research site located in San Juan, PR to serve as our Principal Investigator on clinical trials. The Principal Investigator is responsible for ensuring subject safety, protocol compliance, data integrity, and high-quality study execution in accordance with FDA regulations, ICH-GCP guidelines, sponsor requirements, and company standards. 

This role is ideal for a physician who is interested in clinical research, passionate about improving patient access to innovative therapies, and helping expand research opportunities in the community. In addition to clinical and study oversight responsibilities, the Principal Investigator will support business development and community engagement efforts, including attending sponsor meetings, conducting physician outreach, attending community education events, engaging in media interviews, and others that help build awareness of clinical research. 

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:00am - 5:00pm
Location:  Onsite in San Juan, PR (no capabilities for remote or hybrid work)
Reports to:  Site President
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.

The Company

CMRC Headlands is a premier clinical research site conducting Phase II-IV clinical trials in collaboration with global pharmaceutical sponsors. We advance medical innovation while placing patient experience and operational excellence at the heart of our mission. 

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do. 

Responsibilities:

  • Lead and oversee clinical trials conducted at CMR Center, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
  • Eligible for or active unencumbered license to practice as an MD or DO in Puerto Rico required.
  • Must be board-certified or board-eligible.
  • Bilingual in English and Spanish required
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.
  • Experience in obesity, cardiometabolic disease, vaccines, CNS, gastroenterology, rheumatology, nephrology, pediatrics, or other relevant therapeutic areas preferred.
  • Existing patient access, referral network, or community relationships preferred. 

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