Clinical Study Manager

Responsibilities:

• Develops/maintains project timelines.
• Manages distribution, collection, and tracking of regulatory documentation.
• Negotiates study budgets.

Qualifications:

• Bachelor's degree in Biological Sciences or related field.
• 5+ years of relevant clinical trial experience required.
• Familiar with laws, regulations, standards, and guidance governing the conduct of clinical studies.

Benefits:

• Competitive compensation package.
• Benefits and equity program.
• Generous benefits package including medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).