Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ... Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across ...
You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across ...
As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
Clinical Research Nurse, RN
San Juan, PR · On-site
As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and ... Clinical Research Manager Benefits: Our benefits package for full-time employees includes health ...
Clinical Research Nurse, RN
San Juan, PR · On-site
As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and ... Clinical Research Manager Benefits: Our benefits package for full-time employees includes health ...
Medical Assistant, Research Assistant
San Juan, PR · On-site
$17.50 - $22.25/hr
Enter and verify study data in Electronic Data Capture systems, Clinical Trial Management Systems, electronic medical records, and other study databases. * Assist with completion of source documents ...
Medical Assistant, Research Assistant
San Juan, PR · On-site
$17.50 - $22.25/hr
Enter and verify study data in Electronic Data Capture systems, Clinical Trial Management Systems, electronic medical records, and other study databases. * Assist with completion of source documents ...
Clinical Research Pain Management (Part-Time - 8 hrs/week)
San Juan, PR · On-site
$100 - $230/hr
Clinical Research Pain Management (Part-Time - 8 hrs/week) Location: San Juan, Dorado, PR Schedule ... Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and ...
Clinical Research Pain Management (Part-Time - 8 hrs/week)
San Juan, PR · On-site
$100 - $230/hr
Clinical Research Pain Management (Part-Time - 8 hrs/week) Location: San Juan, Dorado, PR Schedule ... Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and ...
Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ... Strong organizational skills and attention to detail, with the ability to manage multiple projects ...
Medical Assistant, Research Assistant
$17.50 - $22.25/hr
Enter and verify study data in Electronic Data Capture systems, Clinical Trial Management Systems, electronic medical records, and other study databases. * Assist with completion of source documents ...
Medical Assistant, Research Assistant
$17.50 - $22.25/hr
Enter and verify study data in Electronic Data Capture systems, Clinical Trial Management Systems, electronic medical records, and other study databases. * Assist with completion of source documents ...
Clinical Research Nephrologist (Part-Time - 8 hrs/week)
San Juan, PR · On-site
$100 - $230/hr
Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and organizational skills * Strong commitment to ethical research and patient-centered care Why Join Us?
Clinical Research Nephrologist (Part-Time - 8 hrs/week)
San Juan, PR · On-site
$100 - $230/hr
Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and organizational skills * Strong commitment to ethical research and patient-centered care Why Join Us?
Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and organizational skills * Strong commitment to ethical research and patient-centered care Why Join Us?
Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and organizational skills * Strong commitment to ethical research and patient-centered care Why Join Us?
Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and organizational skills * Strong commitment to ethical research and patient-centered care Why Join Us?
Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and organizational skills * Strong commitment to ethical research and patient-centered care Why Join Us?
Clinical Research Manager Benefits: Our benefits package for full-time employees includes health ... Experience preparing for and interacting with clinical trial monitors a plus
Clinical Research Manager Benefits: Our benefits package for full-time employees includes health ... Experience preparing for and interacting with clinical trial monitors a plus
Senior Director, R&D GxP Audit
Juncos, PR · On-site
Oversee audits of clinical trial processes, pharmacovigilance systems, laboratories, quality ... Risk Management & Governance * Use quality risk management principles and data analytics to ...
Senior Director, R&D GxP Audit
Juncos, PR · On-site
Oversee audits of clinical trial processes, pharmacovigilance systems, laboratories, quality ... Risk Management & Governance * Use quality risk management principles and data analytics to ...
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. * Performs clinical study site management/monitoring activities in compliance with ICH ...
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. * Performs clinical study site management/monitoring activities in compliance with ICH ...
Clinical Trial Manager information
What does a clinical trial manager do?
A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.
What does a clinical trial manager do?
A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.
What are the key skills and qualifications needed to thrive as a clinical trial manager, and why are they important?
To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.
What are some common challenges clinical trial managers face when coordinating multi-site studies?
Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.
How much does a clinical trial manager earn?
A clinical trial manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory requirements and project management tools.
What qualifications do you need to be a clinical trial manager?
A clinical trial manager typically needs a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project management. Many roles also require knowledge of Good Clinical Practice (GCP) guidelines and proficiency with trial management software. Advanced degrees or certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.
More about Clinical Trial Manager jobs
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The most popular types of Clinical Trial jobs in Puerto Rico are:
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For Clinical Trial Manager jobs in Puerto Rico, the most frequently searched job titles are:
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The top searched job categories for Clinical Trial Manager jobs in Puerto Rico are:
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Other
Re-posted 17 days ago
Job description
Title: Clinical Research Endocrinologist
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 Endocrinology.
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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