Clinical Research Coordinator III Job Keller area,Texas USA,Healthcare

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