Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Lead and oversee clinical trials conducted at CMR Center, ensuring compliance with protocol ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
Lead and oversee clinical trials conducted at CMR Center, ensuring compliance with protocol ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
Clinical Research Pain Management (Part-Time - 8 hrs/week)
San Juan, PR · On-site
$100 - $230/hr
This is a unique opportunity to contribute your expertise to cutting-edge Pain Management-focused and multi-therapeutic clinical trials , working in a highly collaborative and well-supported research ...
Clinical Research Pain Management (Part-Time - 8 hrs/week)
San Juan, PR · On-site
$100 - $230/hr
This is a unique opportunity to contribute your expertise to cutting-edge Pain Management-focused and multi-therapeutic clinical trials , working in a highly collaborative and well-supported research ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Lead and oversee clinical trials conducted at CMR Center, ensuring compliance with protocol ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
Lead and oversee clinical trials conducted at CMR Center, ensuring compliance with protocol ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
... clinical trials. We're seeking a Clinical Research Nurse (RN) for our clinical research site ... Clinical Research Manager Benefits: Our benefits package for full-time employees includes health ...
... clinical trials. We're seeking a Clinical Research Nurse (RN) for our clinical research site ... Clinical Research Manager Benefits: Our benefits package for full-time employees includes health ...
Clinical Research Nurse, RN
San Juan, PR · On-site
... clinical trials. We're seeking a Clinical Research Nurse (RN) for our clinical research site ... Clinical Research Manager Benefits: Our benefits package for full-time employees includes health ...
Clinical Research Nurse, RN
San Juan, PR · On-site
... clinical trials. We're seeking a Clinical Research Nurse (RN) for our clinical research site ... Clinical Research Manager Benefits: Our benefits package for full-time employees includes health ...
Adaptability, Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring ...
Adaptability, Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring ...
Adaptability, Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring ...
Adaptability, Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring ...
Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies ...
New
Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies ...
New
Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies ...
Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies ...
Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies ...
New
Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies ...
New
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Florida, PR · On-site
Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies ...
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Florida, PR · On-site
Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies ...
CRA 2/Senior CRA 1
San Juan, PR · On-site
$76K - $175K/yr
... high-quality clinical trials. In this role, you'll partner with investigative sites and cross ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...
CRA 2/Senior CRA 1
San Juan, PR · On-site
$76K - $175K/yr
... high-quality clinical trials. In this role, you'll partner with investigative sites and cross ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...
CRA 2/Senior CRA 1
San Juan, PR · On-site
$76K - $175K/yr
... high-quality clinical trials. In this role, you'll partner with investigative sites and cross ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...
CRA 2/Senior CRA 1
San Juan, PR · On-site
$76K - $175K/yr
... high-quality clinical trials. In this role, you'll partner with investigative sites and cross ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...
Clinical Trials Manager information
What does a clinical trials manager do?
A Clinical Trials Manager oversees the planning, coordination, and execution of clinical trials to ensure they are conducted safely, efficiently, and in compliance with regulatory requirements. They manage teams, budgets, timelines, and communication between stakeholders such as sponsors, investigators, and regulatory bodies. Their responsibilities also include monitoring trial progress, resolving issues, and ensuring data integrity throughout the study.
What are some common challenges faced by clinical trials managers and how can they be addressed?
Clinical Trials Managers often encounter challenges such as ensuring regulatory compliance, managing complex timelines, and coordinating communication among diverse stakeholders. Balancing the needs of sponsors, investigators, and regulatory bodies requires strong organizational skills and attention to detail. Proactively addressing these challenges involves implementing robust project management tools, maintaining clear documentation, and fostering open communication within the team. Building relationships with site staff and regularly updating all parties can help anticipate issues early and keep trials on track.
What are the key skills and qualifications needed to thrive as a clinical trials manager, and why are they important?
To thrive as a Clinical Trials Manager, you need expertise in clinical research processes, regulatory compliance, and project management, often supported by a degree in life sciences and experience in clinical trial coordination. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring protocol adherence. These skills and qualities are crucial for maintaining trial integrity, regulatory compliance, and successful project outcomes.
What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?
| Aspect | Clinical Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Oversees entire clinical trial process, manages teams, ensures compliance, and handles budgets. | Assists with patient recruitment, data collection, and site coordination under supervision. |
| Required Credentials | Bachelor’s or higher in life sciences, often with project management experience. | Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred. |
| Work Environment | Works in clinical trial sites, research organizations, or pharmaceutical companies. | Primarily works at clinical sites, hospitals, or research facilities. |
In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.
What are the most commonly searched types of Clinical Trials jobs in Puerto Rico?
The most popular types of Clinical Trials jobs in Puerto Rico are:
What are popular job titles related to Clinical Trials Manager jobs in Puerto Rico?
For Clinical Trials Manager jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Clinical Trials Manager jobs in Puerto Rico look for?
The top searched job categories for Clinical Trials Manager jobs in Puerto Rico are:
Other
Re-posted 17 days ago
Job description
Part-Time Psychiatrist
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 Psychiatry.
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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.
For more info, please reach out:
(210) 624-8683 | manisha.palli@protouchstaffing.com
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