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Key Responsibilities:
- Lead clinical research project planning, execution, and delivery, ensuring regulatory compliance and quality.
- Coordinate cross-functional teams and manage timelines, budgets, and study documentation.
- Act as primary sponsor contact and provide regular progress reports to stakeholders.
Skills & Qualifications:
- Bachelor's degree in health sciences or clinical research with 1-3 years of study management experience.
- Strong knowledge of clinical processes, regulations, and documentation standards.
- Excellent communication, organizational, and problem-solving skills.
What We Offer:
- Education reimbursement, phone and remote work allowances, and office setup support.
- Flexible summer hours, a working-while-visiting program, and referral incentives.
- Eligibility for STIP bonuses and mentorship or leadership development programs.
Alimentiv
Alimentiv is a global CRO advancing therapies for gastrointestinal diseases, with deep expertise in IBD drug development. With about 700 employees across multiple countries, it is a private, profit-with-purpose company focused on scientific research and its people.