Clinical Research Coordinator II Job at Helios Clinical Research, Sherwood, AR

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  • Helios Clinical Research
  • Sherwood, AR

Job Description

Job Title: Clinical Research Coordinator II

FSLA Classification : Non-Exempt

Reports to : Site Operations Manager

Job Summary/ Objective:

 

The Clinical Research Coordinator II 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:

o Ensure trouble-free running of clinical trials.

o Monitor study participants’ health throughout the trial.

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

o Oversee 3-4 trials

• Data Collection and Analysis:

o Collect data obtained from research.

o Analyze research data.

• Participant Interaction:

o Communicate with study participants regarding study objectives.

o Administer questionnaires.

o Monitor participant adherence to study rules.

• Collaboration and Compliance:

o Liaise with laboratories

o Monitor study compliance with protocols and ethical standards.

o Ensure adherence to regulatory requirements.

• Record Keeping:

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

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

• Logistics and Supplies:

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

Education/Experience/Skills

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

Experience: 2 years of experience in Clinical Research

 

Skills:

• Regulatory

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

• Finance

o Stipend payments

• Subject Interaction

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

o Obtain Informed Consent

o Collect medical history

o Conduct study visits

• Administrative

o Source documentation

o EDC

o Query resolution

o AE/SAE documentation and reporting

o Address protocol violations and deviations

o Order supplies

• Clinical Skills

o Phlebotomy

o Vital Signs

o ECG

Working Conditions/ Physical Demands:

Standard operating hours are Monday through Friday, 8:00 a.m. to 5:00 p.m. May 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

Job Tags

Work at office, Monday to Friday,

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