Clinical Project Coordinator

Responsibilities

• Maintains the study file.
• Communicates found or potential problems to study lead or per Communication/Study Plan.
• Performs quality control checks.
• Drafts and assists in the development of study documents for study lead review.
• Tracks and reports study metrics.
• Manages sample tasks.

Qualifications

• Bachelor’s degree in life science or related field, or four years of relevant equivalent work experience.
• Relevant experience in laboratory or clinical study discipline.
• High attention to detail and great oral/written communication skills.
• Ability to work well in a cross-functional team environment.
• Experience with Microsoft 365 programs.

Physical Requirements

• Sitting.
• Talking.
• Hearing.
• Standing.
• Walking.
• Using hands to finger, handle, or feel.
• Reaching with hands and arms.
• Stooping.
• Kneeling.
• Crouching.
• Lifting and/or moving up to 25 pounds.
• Close vision.
• Distance vision.
• Depth perception.

Applicant Requirements

• (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder).

Company Information

• We take geographic location into account when determining base salary to ensure equitable and competitive compensation.
• We are an equal opportunity employer and place a high value on diversity and inclusion at our company.
• We make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as any mental health or physical disability needs.