CMR Center | Full-Time | Clinical Research We're seeking an experienced physician for our clinical ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
CMR Center | Full-Time | Clinical Research We're seeking an experienced physician for our clinical ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
Clinical Research Nurse (RN) Location: San Juan, PR | Site Name: CMR Center | Full-Time Are you an ... Prepare for monitoring visits and assist during sponsor or regulatory audits * Other duties as ...
Clinical Research Nurse (RN) Location: San Juan, PR | Site Name: CMR Center | Full-Time Are you an ... Prepare for monitoring visits and assist during sponsor or regulatory audits * Other duties as ...
Clinical Research Nurse, RN
San Juan, PR · On-site
Clinical Research Nurse (RN) Location: San Juan, PR | Site Name: CMR Center | Full-Time Are you an ... Prepare for monitoring visits and assist during sponsor or regulatory audits * Other duties as ...
Clinical Research Nurse, RN
San Juan, PR · On-site
Clinical Research Nurse (RN) Location: San Juan, PR | Site Name: CMR Center | Full-Time Are you an ... Prepare for monitoring visits and assist during sponsor or regulatory audits * Other duties as ...
Medical Assistant, Research Assistant
$17.50 - $22.25/hr
CMR Center | Full-Time | Clinical Research We're seeking a Medical Assistant for our clinical research site located in San Juan, PR. This role is ideal for someone with direct patient care experience ...
Medical Assistant, Research Assistant
$17.50 - $22.25/hr
CMR Center | Full-Time | Clinical Research We're seeking a Medical Assistant for our clinical research site located in San Juan, PR. This role is ideal for someone with direct patient care experience ...
Medical Assistant, Research Assistant
San Juan, PR · On-site
$17.50 - $22.25/hr
CMR Center | Full-Time | Clinical Research We're seeking a Medical Assistant for our clinical research site located in San Juan, PR. This role is ideal for someone with direct patient care experience ...
Medical Assistant, Research Assistant
San Juan, PR · On-site
$17.50 - $22.25/hr
CMR Center | Full-Time | Clinical Research We're seeking a Medical Assistant for our clinical research site located in San Juan, PR. This role is ideal for someone with direct patient care experience ...
PR · On-site
Identify customer needs, clarify information, research each situation, and provide appropriate ... Provide support for other Nurse Advice Line projects. * Ensure confidentiality and compliance with ...
Quick apply
PR · On-site
Identify customer needs, clarify information, research each situation, and provide appropriate ... Provide support for other Nurse Advice Line projects. * Ensure confidentiality and compliance with ...
Quick apply
PR · On-site
Identify customer needs, clarify information, research each situation, and provide appropriate ... Provide support for other Nurse Advice Line projects. * Ensure confidentiality and compliance with ...
Quick apply
PR · On-site
Identify customer needs, clarify information, research each situation, and provide appropriate ... Provide support for other Nurse Advice Line projects. * Ensure confidentiality and compliance with ...
Quick apply
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 ...
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 ...
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 ...
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 ...
For Project Management services in the Manufacturing and Engineering area. WHAT MAKES YOU A FIT ... Support: Assist with technical, financial, and organizational challenges by researching issues ...
For Project Management services in the Manufacturing and Engineering area. WHAT MAKES YOU A FIT ... Support: Assist with technical, financial, and organizational challenges by researching issues ...
Clinical Specialist - TLAC PR
Caguas, PR · On-site
Collaborates with internal teams on the research, development, implementation and maintaining of ... projects and products. Advises management of any product or performance issues as they arise.
Clinical Specialist - TLAC PR
Caguas, PR · On-site
Collaborates with internal teams on the research, development, implementation and maintaining of ... projects and products. Advises management of any product or performance issues as they arise.
Collaborates with internal teams on the research, development, implementation and maintaining of ... projects and products. Advises management of any product or performance issues as they arise.
Collaborates with internal teams on the research, development, implementation and maintaining of ... projects and products. Advises management of any product or performance issues as they arise.
Collaborates with internal teams on the research, development, implementation and maintaining of ... projects and products. Advises management of any product or performance issues as they arise.
Collaborates with internal teams on the research, development, implementation and maintaining of ... projects and products. Advises management of any product or performance issues as they arise.
... research collaborations such as investigator-initiated trials and collaboration with Clinical Development colleagues on investigator selection, relationship, and site performance/recruitment * Assist ...
... research collaborations such as investigator-initiated trials and collaboration with Clinical Development colleagues on investigator selection, relationship, and site performance/recruitment * Assist ...
... research collaborations such as investigator-initiated trials and collaboration with Clinical Development colleagues on investigator selection, relationship, and site performance/recruitment * Assist ...
... research collaborations such as investigator-initiated trials and collaboration with Clinical Development colleagues on investigator selection, relationship, and site performance/recruitment * Assist ...
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 ...
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 ...
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 ...
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 ...
Clinical Research Project Assistant information
What is the difference between Clinical Research Project Assistant vs Clinical Research Coordinator?
| Aspect | Clinical Research Project Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plus | Requires a bachelor's degree; certifications such as CCRP or CCR are common |
| Work Environment | Supports research teams in clinical settings, hospitals, or research institutions | Manages daily clinical trial activities, interacts directly with patients and investigators |
| Employer & Industry Usage | Used by research institutions, hospitals, pharmaceutical companies | Commonly 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.
What does a clinical research project assistant do?
A clinical research project assistant supports the planning, coordination, and management of clinical trials by assisting with data collection, documentation, and communication among research teams. They often handle administrative tasks, ensure compliance with protocols, and may use tools like electronic data capture systems. Strong organizational skills and attention to detail are essential for this role.
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:
Full-time
Medical, Dental, Vision, Life, PTO
Re-posted 5 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.