Clinical Research Coordinator Experience Certificate

Clinical Research Coordinator Experience Certificate Template
This free clinical research coordinator work experience certificate sample will help you to know how to format a template and write job experience letter to be used as a confirmed document by your ex-employee. View our simple work experience certificate/letter example for clinical research coordinator.

» Clinical Research Coordinator Related Example

Name of the person:______________
Address: ______________
Date: ________

To Whom It May Concern:

This is to certify that ...[ employee title ] ... [ employee name ] was working at ...[ organization name ] as "clinical research coordinator" from ... [ joining date ] to ...[ last working date ].

During this period, his services were found to be satisfactory in carrying out the job duties.

Work Responsibilities - were to:

1) Solicit industry-sponsored trials through contacts professional organizations

2) Register protocol patients with appropriate statistical centers as required

3) Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups

4) Participate in preparation and management of research budgets monetary disbursements

5) Perform specific protocol procedures like interviewing subjects, taking vital signs, and performing electrocardiograms

6) Interpret protocols advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics

7) Develop advertising other informational materials to be used in subject recruitment

8) Contact industry representatives to make sure equipment software specifications necessary for successful study completion

9) Confer with health care professionals to define the best recruitment practices for studies

10) Track enrollment status of subjects and document dropout information like dropout causes subject contact efforts

11) Review proposed study protocols to evaluate factors like sample collection processes, data management plans, and potential subject risks

12) Record adverse event and side effect data confer with investigators regarding the reporting of events to oversight agencies

13) Prepare study-related documentation like protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports

14) Participate in the development of study protocols including guidelines for administration or data collection procedures

15) Oversee subject enrollment to make sure that informed consent is properly obtained documented

16) Order drugs or devices necessary for study completion

17) Organize space for study equipment supplies

18) Maintain contact with sponsors to schedule coordinate site visits or to answer questions about issues like incomplete data

19) Instruct research staff in scientific procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures

20) Inform patients or caregivers about study aspects outcomes to be expected

21) Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts like protocol revisions

22) Dispense medical devices or drugs, and calculate dosages provide instructions as necessary

23) Direct the requisition, collection, labeling, storage, or shipment of specimens

24) Contact outside health care providers communicate with subjects to obtain follow-up information

25) Communicate with laboratories or investigators regarding laboratory findings

26) Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions

27) Code, evaluate, or interpret collected study data

28) Assess eligibility of potential subjects through methods like screening interviews, reviews of medical records, and discussions with physicians nurses

29) Arrange for research study sites determine staff or equipment availability

30) Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols

31) Monitor study activities to make sure compliance with protocols and with all relevant local, federal, and state regulatory institutional polices

32) Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms

We wish him/her all the best in his future

...[ Employer name ]
...[ Employer position ]
...[ Organization sign/stamp ]

See also

Read more experience letter articles in our blog.

Share on Facebook Share on Twitter Share on LinkedIn
Back to top

Home | Privacy Policy | Terms of Use

Copyright 2011 - 2020 - All Rights Reserved