Clinical Research Coordinator III

Jimmy Jazz; Keller (TX); On-site; USD 65,000 - 85,000; Full time

Job summary

Jimmy Jazz is seeking a Clinical Research Coordinator III to support the management and oversight of multiple clinical trials at the Keller, TX site. You will work under the Site Operations Manager to ensure trials run smoothly and comply with regulatory standards.

The role emphasizes data collection, participant interaction, and collaboration with laboratories to uphold study integrity and patient safety.

Qualifications

• Bachelor's degree preferred in health-related field.
• Minimum 3 years experience in Clinical Research preferred.
• Experience with clinical trials and regulatory compliance.
• Ability to recruit and interact with study participants.

Responsibilities

• Oversee clinical trials to ensure smooth execution and compliance.
• Collect and manage data from studies including case report forms.
• Interact with study participants to explain objectives and ensure adherence.
• Coordinate with laboratories and ensure protocol adherence and regulatory compliance.
• Maintain accurate research records including drug dispensation and sample handling.
• Manage supplies and equipment to support trials and site operations.
• Take part in feasibility assessments, start-up visits, and trial closeouts.

Skills

Filing and accessing documents

Study Submission Assistant

Close out Visits

Education

Bachelor's degree preferred in health-related field

Tools

EDC

Job description

• Location 300 N Rufe Snow Drive,Keller, TX, 76248,United States


• Employee Type Non-Exempt - FT

J ob Title : Clinical Research Coordinator I I I

FLSA Classification: Non - Exempt

Reports to: Site Operations Manager

Job Summary / Objective :

The Clinical Research Coordinator I I I is responsible for supporting the management and oversight of clinical trials. This role involves working closely with a team to ensure the smooth execution of research studies under the guidance of the Site Operations Manager

Essential Functions :

Overseeing Clinical Trials:

• Ensure trouble-free running of clinical trials.


• Monitor study participants’ health throughout the trial.


• Compile reports summarizing the success or failure of drugs, technologies, or medical procedures


• Oversee 5+ trials

Data Collection and Analysis:

• Collect data obtained from research.

Participant Interaction:

• Communicate with study participants regarding study objectives .


• Monitor participant adherence to study rules.

Collaboration and Compliance:

• Liaise with laboratories


• Monitor study compliance with protocols and ethical standards.


• Ensure adherence to regulatory requirements.

Record Keeping:

• Maintain research records, including case report forms and drug dispensation records.


• Direct specimen collection, labeling, storage, and transport.

Logistics and Supplies:

• Ensure all necessary equipment and supplies are in stock and functional.

Education/Experience/Skills

Education : Bachelor's degree preferred in health-related field

Experience : 3 years experience in Clinical Research preferred

Skills:

• Filing and accessing documents, Study Submission Assistant , Conduct Close out Visits

Finance

• Stipend payme nts

Subject Interaction

• Recruit, interview, screen , enroll , and randomize subjects


• Collect medical history
  
• Conduct study visits

Administrative

• EDC


• Query resolution


• AE/SAE documentation and reporting


• Ad d ress protocol violations and deviations


• Order supplies

Clinical Skills

• Vital Sign s


• E C G

Study Management

• Conduct PSSV’s and SIV’s


• Complete Feasibility Questionnaires


• Manage trials from start to closeout

Working Conditions / Physical Demands: Standard operating hours are Monday through Friday, 8:00 a.m. to 5 : 00 p.m . M ay be required to complete job-related tasks outside of that time frame in excess of a standard 40-hour work week . Requires prolonged walking, standing, some bending , stooping, and stretching . Requires hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment . Requires normal range of hearing and eyesight to record, prepare , and communicate appropriate reports .

Travel required: as needed (travel to IM’s may be required )

Disclaimer

T his job description may not be inclusive of all assigned duties, responsibilities , or aspects of the jo b described , and may be amended at any time at the sole discretion of the Employer