Clinical Research Obesity Medicine Physician San Juan, PR | ⏰ Part-Time (0-8 hours/week) About the Role We are seeking a Board-Certified Physician to join as a Clinical Research Physician ...
Clinical Research Obesity Medicine Physician San Juan, PR | ⏰ Part-Time (0-8 hours/week) About the Role We are seeking a Board-Certified Physician to join as a Clinical Research Physician ...
Registered Nurse
$38K/yr
... facilities performing clinical or research training experiences to satisfy program or degree ... Credit for foreign nursing education higher that associate degree/entry level requires a formal ...
Registered Nurse
$38K/yr
... facilities performing clinical or research training experiences to satisfy program or degree ... Credit for foreign nursing education higher that associate degree/entry level requires a formal ...
HEMODIALYSIS NURSE MANAGER
San Juan, PR · On-site
$92K/yr
Functions as a clinical expert and is responsible and accountable for all elements of the nursing ... Credit for foreign nursing education higher that associate degree/entry level requires a formal ...
HEMODIALYSIS NURSE MANAGER
San Juan, PR · On-site
$92K/yr
Functions as a clinical expert and is responsible and accountable for all elements of the nursing ... Credit for foreign nursing education higher that associate degree/entry level requires a formal ...
Clinical Research Associate information
What is a clinical research associate?
Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.
What are the key skills and qualifications needed to thrive as a clinical research associate?
To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.
What are some common challenges clinical research associates face when monitoring clinical trial sites?
Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.
What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?
| Aspect | Clinical Research Associate | Clinical Trial Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often with clinical research certifications | Bachelor's degree, often with clinical research or healthcare certifications |
| Work Environment | Monitors clinical sites, reviews data, ensures compliance | Coordinates trial activities, manages schedules, and communicates with sites |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, CROs |
Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.
Is being a clinical research associate worth it?
A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.
Is it hard to get a clinical research associate job?
Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Puerto Rico?
The most popular types of Clinical Research jobs in Puerto Rico are:
What job categories do people searching Clinical Research Associate jobs in Puerto Rico look for?
The top searched job categories for Clinical Research Associate jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Clinical Research Associate jobs?
Cities in Puerto Rico with the most Clinical Research Associate job openings:
Other
Re-posted 17 days ago
Job description
Title: Clinical Research Obesity Medicine Physician
About the Role
Key Responsibilities
Qualifications
Benefits
San Juan, PR | ⏰ Part-Time (0-8 hours/week)
About the Role
We are seeking a Board-Certified Physician to join as a Clinical Research Physician supporting Phase I-IV clinical trials in San Juan, PR. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies.
Key Responsibilities
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Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.
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Conduct medical screenings, physical exams, and assessments of study participants.
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Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.
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Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.
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Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
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Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.
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Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.
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Contribute to feasibility reviews, study design, and recruitment strategies.
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Stay current with clinical research regulations and therapeutic advances.
Qualifications
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M.D. or D.O. with an active, unrestricted PR medical license.
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Board Certification in Obesity Medicine.
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Valid DEA license and BLS/ACLS certification.
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Clinical research/clinical trials experience preferred (training available for motivated candidates).
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Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
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Excellent communication, collaboration, and interpersonal skills.
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Strong commitment to ethical research and patient-centered care.
Benefits
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Flexible, part-time schedule (0-8 hours per week).
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Opportunity to expand expertise in multi-therapeutic clinical trials.
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Direct involvement in advancing innovative treatments through research.
About Protouch Staffing
Sourced by ZipRecruiter
Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Frisco, TX, US
Year founded
1989