Complete the CRA Training Program (12-14 weeks) to gain the skills needed as a primary CRA.
Conduct site visits (PSSV, SIV, IMV, COV) and manage site performance, data quality, and patient safety.
Build strong relationships with site personnel and ensure effective communication with the Clinical Study Team.
BeOne is a global oncology company discovering and developing innovative, affordable treatments for cancer patients worldwide. Our growing global team of more than 11,000 colleagues fosters a collaborative, patients-first culture.
Take ownership of clinical project delivery, ensuring contracted deliverables are met while managing quality, timelines, and budgets.
Lead communication and collaboration with clients, project managers, functional leads, vendors, and clinical teams worldwide.
Mentor team members, use data-driven tools to anticipate risks, and drive continuous improvement in study execution.
Our partner is a specialized clinical research organization focused on advancing pharmaceutical and medical device development. They foster a multicultural, matrixed environment emphasizing quality, collaboration, and innovation.
Leads the planning, conduct, and oversight of clinical studies per scope of work, ensuring compliance with protocols, SOPs, and regulatory requirements.
Acts as primary clinical point of contact for clients, develops study documents, and drives site feasibility and recruitment strategies.
Manages clinical teams, training, vendor oversight, and ensures data quality and timely deliverables across study phases.
Precision Medicine Group is a clinical research organization that provides outsourced clinical trial management services to pharmaceutical and biotechnology companies. The company fosters a collaborative culture focused on quality and compliance, and employs a team of experienced clinical professionals.