Employer Industry: Clinical Research

Why Consider this Job Opportunity:
- Competitive salary
- Opportunity for career growth and advancement within the organization
- Remote work flexibility
- Supportive and collaborative work environment
- Chance to contribute to the safety and efficiency of clinical trials

What to Expect (Job Responsibilities):
- Conduct accurate pre-review of new and revised consent forms in regulatory compliance
- Edit consent forms to ensure regulatory compliance and alignment with document standards
- Apply negotiated Sponsor language to consent form documents
- Collaborate with Board members and staff to incorporate necessary edits to consent forms
- Maintain and increase regulatory knowledge to assist with organizational compliance

What is Required (Qualifications):
- Associate's degree (preferred)
- Minimum of two years of experience in technical/medical writing and/or editing
- Proficiency in Word processing and editing
- Familiarity with Excel, PowerPoint, direct messaging applications, remote meeting applications, and web-based proprietary software
- Excellent communication skills, both verbal and written

How to Stand Out (Preferred Qualifications):
- 0-2 years of experience in clinical research or related field

#ClinicalResearch #MedicalWriting #RegulatoryCompliance #RemoteWork #CareerGrowth

We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.