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)
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) 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) Location: San Juan, Dorado, PR Schedule ... Proficient in EHR systems and clinical trial platforms (EDC, CTMS) * Excellent communication and ...
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 ...
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 ...
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
Sr. Account Manager
Cayey, PR · On-site
$110 - $170/hr
As a Sr Account Manager at Thermo Fisher Scientific, you will increase revenue by developing and managing strategic customer relationships across our diverse portfolio of scientific products and ...
New
Sr. Account Manager
Cayey, PR · On-site
$110 - $170/hr
As a Sr Account Manager at Thermo Fisher Scientific, you will increase revenue by developing and managing strategic customer relationships across our diverse portfolio of scientific products and ...
New
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 ...
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 ...
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 ...
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 ...
PR · On-site
... Manager) by coordinating service-related activities such as parts availability, demos, services ... Create contract records in Acumatica for billing on the first day of each month and distribute ...
Quick apply
PR · On-site
... Manager) by coordinating service-related activities such as parts availability, demos, services ... Create contract records in Acumatica for billing on the first day of each month and distribute ...
Contract Clinical Trial Manager information
What is a contract clinical trial manager?
A Contract Clinical Trial Manager is a professional who oversees the planning, execution, and management of clinical trials for pharmaceutical, biotech, or medical device companies on a contractual basis. Unlike full-time employees, contract clinical trial managers are typically hired for specific projects or time periods to ensure compliance with regulatory requirements, manage study timelines, and coordinate with cross-functional teams. Their responsibilities include supervising site selection, budget management, and ensuring data quality and patient safety throughout the trial. They play a crucial role in bringing new treatments to market by ensuring trials are conducted efficiently and ethically.
What are the key skills and qualifications needed to thrive as a contract clinical trial manager?
To thrive as a Contract Clinical Trial Manager, you need expertise in clinical research processes, project management, regulatory compliance, and a degree in life sciences or related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications such as ACRP or SOCRA are commonly required. Excellent organizational skills, attention to detail, and strong communication enable effective coordination with sponsors, sites, and cross-functional teams. These skills ensure clinical trials meet regulatory standards, timelines, and quality benchmarks critical for successful drug development.
What are some common challenges faced by contract clinical trial managers, and how can they be effectively addressed?
Contract Clinical Trial Managers often navigate challenges such as coordinating multiple stakeholders, adhering to tight timelines, and managing protocol deviations across diverse research sites. To address these, strong communication skills and proactive project management are essential. Developing clear processes for documentation, regular team check-ins, and maintaining flexibility help ensure that trials remain compliant and on schedule. Additionally, leveraging technology for real-time data tracking can streamline collaboration and issue resolution.
What is the difference between Contract Clinical Trial Manager vs Clinical Research Associate?
| Aspect | Contract Clinical Trial Manager | Clinical Research Associate |
|---|---|---|
| Credentials | Typically requires a Bachelor's degree in life sciences, clinical research certification preferred | Usually holds a Bachelor's degree in life sciences or related field, with some certifications |
| Work Environment | Manages multiple trials, oversees teams, often works remotely or on-site at trial locations | Monitors clinical sites, ensures protocol compliance, works primarily on-site at trial locations |
| Employer & Industry Usage | Hired by pharmaceutical companies, CROs, or biotech firms for trial management | Employed by sponsors or CROs to monitor and support clinical sites |
The Contract Clinical Trial Manager focuses on overseeing entire clinical trials, managing teams, and ensuring trial milestones are met. In contrast, the Clinical Research Associate primarily monitors clinical sites to ensure compliance and data integrity. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.
What are popular job titles related to Contract Clinical Trial Manager jobs in Puerto Rico?
For Contract Clinical Trial Manager jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Contract Clinical Trial Manager jobs in Puerto Rico look for?
The top searched job categories for Contract Clinical Trial Manager jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Contract Clinical Trial Manager jobs?
Cities in Puerto Rico with the most Contract Clinical Trial Manager job openings:
Other
Re-posted 20 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