What are the responsibilities and job description for the Oncology - Clinical Research Coordinator II position at Helios Clinical Research?
This is for our location in Lakeland, Florida. Candidates must be local.
Prior experience in Oncology Research is required!
Job Title: Clinical Research Coordinator
FLSA Classification: Non-Exempt
Reports to: Site Operations Manager
Job Summary/ Objective:
The Clinical Research Coordinator 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 1-2 trials
Data Collection and Analysis:
- Collect data obtained from research.
- Analyze research data.
Participant Interaction:
- Communicate with study participants regarding study objectives.
- Administer questionnaires.
- 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: 1-year experience in Clinical Research
Skills
Regulatory
- Filing and accessing documents, Study Submission Assistant
Finance
- Stipend payments
Subject Interaction
- Recruit, interview, screen, enroll, and randomize subjects
- Obtain Informed Consent
- Collect medical history
- Conduct study visits
Administrative
- Source documentation
- EDC
- Query resolution
- AE/SAE documentation and reporting
- Address protocol deviations
- Order supplies
Clinical Skills
- Phlebotomy
- Vital Signs
- 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)