Senior Clinical Research Associate (East Coast)

Job Overview:

• Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities.
• Ensure investigational sites have adequate facilities, staff, and resources for study conduct.

Qualifications:

• Degree in Life Sciences or equivalent education and experience.
• Extensive on-site monitoring experience in phase 2/3 trials, preferably in oncology or rare disease.

Responsibilities:

• Train site staff and support regulatory/EC submissions.
• Mentor and co-monitor junior staff to assess performance.

Company Culture:

• Emphasizes values like quality, integrity, drive, agility, belonging, and collaboration.
• Encourages professional growth and making a difference in patients' lives.