A prestigious organization is looking for a Business Analyst to join its team in a Senior and Remote role. This role is integral to managing clinical trial documentation and regulatory submissions.
About the Opportunity:
- Assignment Length: 13 weeks
- Schedule: Full-time
- Hours: Standard business (40 hours per week)
- Setting: Remote
Responsibilities:
- Leading the end-to-end process for authoring clinical trial documentation and regulatory submissions
- Collaborating with cross-functional teams to gather and document business requirements
- Facilitating requirements gathering workshops
- Authoring comprehensive SDLC documentation
- Ensuring compliance with regulatory standards and internal quality processes
Qualifications:
- 8+ years of experience in Business Analysis or related roles
- Bachelor’s Degree in a related field
- Experience with Clinical Trial documentation
- Proficiency in SDLC methodologies
- Excellent communication skills
- Problem-solving abilities
- Strong organizational skills
- Attention to detail
- Team collaboration skills
Desired Skills:
- 10 years of experience in the Life Sciences industry
- Bachelor’s Degree in Life Sciences
- Certification in Business Analysis
- Advanced knowledge of regulatory standards
- Strong facilitation and stakeholder management skills
