Research Protocol Analyst (Remote) - Clinical Research Protections

Talentify.io; United States; Remote; USD 60,000 - 90,000; Full time

Job summary

Talentify.io seeks a qualified individual to manage human research protocols in a fully remote role. This position offers opportunities for career advancement and involvement in vital research that influences treatment for serious illnesses. Candidates must have a bachelor's degree and relevant experience in clinical research.

Qualifications

• Bachelor's degree with at least 2 years of experience in clinical research review.
• Knowledge of federal and state regulations related to research subjects.
• Certified IRB Professional (CIP) preferred.

Responsibilities

• Manage human research protocols from submission through their life cycle.
• Prepare materials for committee meetings and ensure compliance.
• Participate in quality improvement initiatives.

Skills

Interpersonal Skills

Compliance Management

Quality Improvement

Education

Bachelor's degree

Tools

Microsoft Office

iMedRIS

Forte's OnCore

Job description

Employer Industry: Biomedical Research and Healthcare

Why consider this job opportunity:
- Fully remote position offering flexibility in work environment
- Opportunity for career advancement and growth within the organization
- Involvement in groundbreaking research that impacts cancer and other life-threatening illnesses
- Collaborative work environment focused on innovative approaches to healthcare
- Competitive salary based on experience, qualifications, and work location

What to Expect (Job Responsibilities):
- Manage a portfolio of human research protocols from submission through the protocol's life cycle
- Shepherd protocols through the Cancer Protocol Review and Monitoring Committee (CPRMC) and Institutional Review Board (IRB) review processes
- Prepare materials for committee meetings, ensuring completeness and relevance
- Assist in preparing materials for internal and external audits and ensure compliance with documentation requirements
- Participate in quality improvement initiatives related to policies, procedures, and workflow updates

What is Required (Qualifications):
- Bachelor's degree with at least 2 years of experience in an academic/clinical research review setting
- Minimum of 5 years of experience may substitute for the educational requirement
- Experience in reviewing and processing research protocols in an academic research setting
- Knowledge of federal and state regulations regarding human and/or animal subjects in research
- Effective interpersonal skills for dealing with complex and sensitive information

How to Stand Out (Preferred Qualifications):
- Certified IRB Professional (CIP) is preferred but not required
- Experience with software related to the role, including Microsoft Office, Outlook, Excel, iMedRIS, and Forte's OnCore

#BiomedicalResearch #HealthcareCareers #RemoteWork #CareerAdvancement #ClinicalResearch

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