... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
Clinical Protocol Developer
Portsmouth, VA · On-site
$23.50 - $31.25/hr
... writing, and producing human and animal research protocols in support of the military medicine ... Work with the data management team, clinical operations team, and other research collaborators in ...
Clinical Protocol Developer
Portsmouth, VA · On-site
$23.50 - $31.25/hr
... writing, and producing human and animal research protocols in support of the military medicine ... Work with the data management team, clinical operations team, and other research collaborators in ...
Coordinate development of research protocols and treatment plans with physicians, pharmacists ... CCRP, CRN-BC, OCN) • Effective problem-solving abilities • Effective communication and writing ...
Coordinate development of research protocols and treatment plans with physicians, pharmacists ... CCRP, CRN-BC, OCN) • Effective problem-solving abilities • Effective communication and writing ...
Clinical Research Coordinator 2
$23.25 - $30.75/hr
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... This role assists in the day-to-day operations of clinical research protocol implementation, and ...
Clinical Research Coordinator 2
$23.25 - $30.75/hr
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... This role assists in the day-to-day operations of clinical research protocol implementation, and ...
Clinical Research Coordinator
Chicago, IL · On-site
$25 - $33.25/hr
Protocol Management * Assist in establishing and coordinating the implementation of clinical research protocol priorities and organization structure. * Notify and inform physicians, clinical staff ...
Clinical Research Coordinator
Chicago, IL · On-site
$25 - $33.25/hr
Protocol Management * Assist in establishing and coordinating the implementation of clinical research protocol priorities and organization structure. * Notify and inform physicians, clinical staff ...
Clinical Research Coordinator 2
Miami, FL · On-site
$23.25 - $30.75/hr
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... This role assists in the day-to-day operations of clinical research protocol implementation, and ...
Clinical Research Coordinator 2
Miami, FL · On-site
$23.25 - $30.75/hr
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... This role assists in the day-to-day operations of clinical research protocol implementation, and ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...
... Temporary Clinical Research Manager at UNC Chapel Hill
... Temporary Clinical Research Manager at UNC Chapel Hill
Clinical Research Nurse
Travis Air Force Base, CA · On-site
$47 - $60/hr
Develop an individualized timeline for each protocol. * Complete the necessary documents for ... by obtaining written informed consent. * Communicate with the IRB point of contact (POC); as ...
Quick apply
Clinical Research Nurse
Travis Air Force Base, CA · On-site
$47 - $60/hr
Develop an individualized timeline for each protocol. * Complete the necessary documents for ... by obtaining written informed consent. * Communicate with the IRB point of contact (POC); as ...
Clinical Research Coordinator 2
Miami, FL · On-site
$23.25 - $30.75/hr
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... This role assists in the day-to-day operations of clinical research protocol implementation and ...
Clinical Research Coordinator 2
Miami, FL · On-site
$23.25 - $30.75/hr
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... This role assists in the day-to-day operations of clinical research protocol implementation and ...
Clinical Research Coordinator 2
$23.25 - $30.75/hr
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... This role assists in the day-to-day operations of clinical research protocol implementation and ...
Clinical Research Coordinator 2
$23.25 - $30.75/hr
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... This role assists in the day-to-day operations of clinical research protocol implementation and ...
Senior Clinical Research Coordinator
Chicago, IL · On-site
$25 - $33.25/hr
Duties & Responsibilities Protocol Management Assist in establishing and coordinating the ... Schedule and conduct clinical research visits required by the protocol and track participant visits.
Senior Clinical Research Coordinator
Chicago, IL · On-site
$25 - $33.25/hr
Duties & Responsibilities Protocol Management Assist in establishing and coordinating the ... Schedule and conduct clinical research visits required by the protocol and track participant visits.
Clinical Research Nurse
Travis Air Force Base, CA · On-site
$47 - $60/hr
Develop an individualized timeline for each protocol. * Complete the necessary documents for ... by obtaining written informed consent. * Communicate with the IRB point of contact (POC); as ...
Quick apply
Clinical Research Nurse
Travis Air Force Base, CA · On-site
$47 - $60/hr
Develop an individualized timeline for each protocol. * Complete the necessary documents for ... by obtaining written informed consent. * Communicate with the IRB point of contact (POC); as ...
Coordinator Clinical Research
Flint, MI · On-site
$23.50 - $31.25/hr
... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...
Coordinator Clinical Research
Flint, MI · On-site
$23.50 - $31.25/hr
... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...
Clinical Research Coordinator
Cincinnati, OH · On-site
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Clinical Research Coordinator
Cincinnati, OH · On-site
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Clinical Research Coordinator
Portsmouth, VA · On-site
$23.50 - $31.25/hr
... each protocol in accordance with written policies and procedures as set forth in Title 21 of the ... Maintain proficiency required to coordinate clinical research such as: communication skills and ...
Clinical Research Coordinator
Portsmouth, VA · On-site
$23.50 - $31.25/hr
... each protocol in accordance with written policies and procedures as set forth in Title 21 of the ... Maintain proficiency required to coordinate clinical research such as: communication skills and ...
Temporary Clinical Research Protocol Writer information
See salary details
$25 - $30.31
10% of jobs
$30.31 - $35.62
9% of jobs
$39.07 is the 25th percentile. Wages below this are outliers.
$35.62 - $40.93
11% of jobs
$40.93 - $46.24
2% of jobs
$46.24 - $51.55
1% of jobs
The median wage is $55.31 / hr.
$51.55 - $56.86
26% of jobs
$56.86 - $62.17
15% of jobs
$63.28 is the 75th percentile. Wages above this are outliers.
$62.17 - $67.48
13% of jobs
$67.48 - $72.79
10% of jobs
$72.79 - $78.10
4% of jobs
$78.10 - $83.41
1% of jobs
$25
$54
$83
How much do temporary clinical research protocol writer jobs pay per hour?
What is the difference between Temporary Clinical Research Protocol Writer vs Temporary Clinical Research Associate?
| Aspect | Temporary Clinical Research Protocol Writer | Temporary Clinical Research Associate |
|---|---|---|
| Primary Role | Develops and writes clinical research protocols and related documents | Monitors and manages clinical trial activities at sites |
| Required Skills | Scientific writing, regulatory knowledge, protocol development | Site management, data collection, compliance monitoring |
| Work Environment | Office-based, collaboration with research teams | Site visits, on-site monitoring, coordination with sites |
| Common Certifications | GCP training, clinical research certifications | GCP training, clinical research certifications |
While both roles support clinical trials, the Temporary Clinical Research Protocol Writer focuses on creating detailed protocols and documentation, whereas the Temporary Clinical Research Associate manages trial execution and site activities. Understanding these differences helps in choosing the right position based on skills and career goals.
Houston Methodist rating
8.1
Based on 293 frontline employees who took The Breakroom Quiz
69th of 872 rated healthcare providers
Job description
Exempt
QUALIFICATIONS
EDUCATION
- Bachelor's degree in Nursing or higher from an accredited school of nursing
EXPERIENCE
- One year acute care or clinical research experience
LICENSES AND CERTIFICATIONS
Required
- RN - Registered Nurse - Texas State Licensure - Texas Board of Nursing_PSV Compact Licensure - Must obtain permanent Texas license within 60 days (if establishing Texas residency) and
- BLS - Basic Life Support or Instructor (AHA) - American Heart Association
SKILLS AND ABILITIES
- Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going skills, competency assessments, and performance evaluations
- Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security
- Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles
- Demonstrates clinical problem solving and critical thinking using an analytical approach
- Adapts to multiple ongoing priorities with minimal supervision including, organizing work flow and actively participating in problem-solving
- Exhibits strong interpersonal and team player skills with all levels of the healthcare team and assures delivery of excellent customer service to all patients, visitors, physicians and co-workers
- Possesses basic computer knowledge; operates multiple computer systems to include, Hospital Information Systems and Office software to maintain patient and exam documents
ESSENTIAL FUNCTIONS
PEOPLE ESSENTIAL FUNCTIONS
- Uses therapeutic communication, which includes active listening and teaching, to provide research interventions care to clinical research patients and coordinates with interprofessional team as written in the research protocol. Contributes to teamwork by consistently responding positively to requests for assistance.
- Provides patient education regarding disease process and involves patient and family in decision-making processes. Consistently evaluates the patient's comprehension and adapts teaching methods accordingly. Advocates on patient/family's behalf to identify and resolve clinical and ethical concerns, utilizing appropriate resources.
- Facilitates onboarding and orientation process for new staff in conjunction with Clinical Trials Manager. Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards improvement of department score for turnover/retention/employee engagement.
SERVICE ESSENTIAL FUNCTIONS
- Demonstrates ability to manage multiple projects at different stages of the clinical research process (Phase 1-Phase 4).
- Coordinates pre-site and site initiation visits; trains hospital and clinic nurses/physicians on scientific aspects and protocol requirements of research studies. Attends off-site investigator meetings.
- Provides comprehensive nursing assessments to develop, coordinate, implement and evaluate activities associated with all phases of clinical research projects. Monitors safety of all research subjects and reports adverse events.
- Helps drive improvement of department score for patient satisfaction, through peer-to-peer accountability to service standards.
QUALITY/SAFETY ESSENTIAL FUNCTIONS
- Follows the clinical research protocol and nursing process and modifies care based on continuous evaluation of the research patient's condition. Performs nursing functions independently and in collaboration with Principal Investigator as approved by Hospital administration for the conduct of clinical research.
- Collects, processes and ships protocol-required lab specimens; maintains supply and equipment inventory; maintains appropriate laboratory certification as well as perform study closeout procedures including post-study documentation, return of study materials to the sponsor and data archiving.
- Collaborates and prepares with Principal Investigator, Institutional Review Board (IRB) and regulatory documents for submission assuring compliance with local and federal regulatory standards as appropriate and required by the research protocol. Follows International Council for Harmonisation/Good Clinical Practice guidelines.
FINANCE ESSENTIAL FUNCTIONS
- Assisting financial analyst in development of calendar and Medicare Cost Analysis. standard of care procedures vs. research and approving study calendars for Clinical Trials Management System.
- Identifies, recruits, and consents clinical research subjects for participation in approved clinical trials; monitors enrollment goals and modifies enrollment strategies, as necessary.
- Enters study related data into Clinical Trials Management System (CTMS) in accordance with Houston Methodist Research Institute policy.
GROWTH/INNOVATION ESSENTIAL FUNCTIONS
- Identifies and presents areas for innovation, efficiency and improvement in patient care operations using evidence-based practice literature. Offers innovative solutions through evidence-based practice/performance improvement projects and activities.
- Maintains accountability for ongoing professional growth and development. Participates in unit activities. Completes and updates the individual development plan (IDP) on an on-going basis.
SUPPLEMENTAL REQUIREMENTS
- WORK ATTIRE
- Uniform: Yes
- Scrubs: Yes
- Business professional: No
- Other (department approved): No
- On Call* No
- May require travel within the Houston Metropolitan area No
- May require travel outside Houston Metropolitan area No
ON-CALL*
*Note that employees may be required to be on-call during emergencies (ie. Disaster, Severe Weather Events, etc) regardless of selection below.
TRAVEL**
**Travel specifications may vary by department**
Work Shift:
1 - Day (United States of America)Job Category:
Non-clinical Houston Methodist is one of the nation's leading health systems and academic medical centers. The health system consists of eight hospitals: Houston Methodist Hospital, its flagship academic hospital in the Texas Medical Center, seven community hospitals and one long-term acute care hospital throughout the Greater Houston metropolitan area. Houston Methodist also includes a research institute; a comprehensive residency program; international patient services; freestanding comprehensive care clinics, emergency care and imaging centers; and outpatient facilities. Come lead with us!Houston Methodist is an Equal Opportunity Employer.
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