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Form of work
Salary- Prepare, submit, and monitor clinical trial subject data under the direction of the Clinical Research Manager.
- Prepare, maintain and organize Regulatory files for each assigned study in compliance with study sponsor requirement.
- Assist in the preparation and coordination of assigned study monitoring and auditing visits with the Clinical Research Manager and sponsors.
- Maintain clinical research staff credentialing files.
- Monitor temperatures and calibration of research equipment.
- Assist with scheduling for research subjects.
- Coordinate ordering of research supplies, such as dry ice, and coordinate Fed-Ex and UPS shipments.
- Maintain working knowledge of current regulations, regulatory guidance and or local policies.
- Assist Clinical Research Manager with regulatory based training and implementation of new or revised regulation, guidance and or local policy.
- Attend clinical research department meetings.
- Other duties as assigned.
Requirements
- Minimum of high school diploma, associates degree preferred.
- Minimum 2 years healthcare experience required. Oncology or prior research experience strongly desired.
- Medical terminology.
- Attention to detail and strong organizational skills.
- Working knowledge of MS Word and Excel.
- Strong communication and interpersonal skills.
- Reliable and punctual.
Please forward resume and cover letter for consideration. All applicants must provide proof of Covid-19 vaccination.
Job Type: Full-time
Pay: $22.00 - $24.00 per hour
Expected hours: 40 per week
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Tuition reimbursement
- Vision insurance
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Ability to Relocate:
- Albany, NY 12208: Relocate before starting work (Required)
Work Location: In person
