What are the responsibilities and job description for the Clinical Research Associate 2064742 position at Stratacuity: Proven Scientific Placement?
Location: Boston, MA (Onsite)
Focus: Oncology
Job Overview: Join our client as the inaugural in-house Clinical Research Associate to oversee quality and patient safety, coordinating with a CRO and facilitating daily study operations.
Primary Job Responsibilities:
- Partner with CROs for trial monitoring, maintaining compliance, data accuracy, and site relations.
- Perform site visits to ensure protocol compliance and manage essential documentation.
- Build relationships with study sites and vendors, and develop monitoring tools for data review.
- Assist in audit support, track enrollment, oversee data collection, and collaborate on study goals.
Primary Job Requirements:
- Bachelor's degree with 6 years of clinical trials experience
- Skilled in managing complex oncology studies with a quality and compliance emphasis.
- Solid understanding of ICH/GCP, regulations, and relationship-building with sites/vendors.
- Willing to travel 50% and adept with Microsoft Office, EDC, CTMS, and eTMF.
About Stratacuity:
Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member. We build lasting relationships with exceptional biopharmaceutical talent and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a Stratacuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.
PROVEN SCIENTIFIC PLACEMENT™
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