Remote Biotech research and development Jobs · MS Office

• Collaborate with the Clinical Operations team to support timely conduct of clinical studies according to protocols, GCP, SOPs, and regulations.
• Lead operational management for assigned regions and sites, including vendor management and oversight of CRO monitors.
• Contribute to the development and maintenance of study documents and ensure the Trial Master File is complete and inspection-ready.

BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines for patients with genetic diseases and cancers with clear genetic drivers. Founded in 2015, the company has built a portfolio of 20+ drug development programs spanning preclinical to late-stage development across multiple therapeutic areas.

• Conduct and report all types of onsite monitoring visits.
• Perform CRF review, source document verification, and query resolution.
• Support study startup, site communication, and audits.

PSI is a leading CRO with 30+ years in the industry, offering stability and innovation. We focus on quality and on-time services across therapeutic indications, with friendly and supportive colleagues.

• Work on the frontline of communication with project stakeholders, ensuring timelines, targets, and standards.
• Build and maintain relationships with clinical sites and investigators, focusing on subjects' rights, safety, and well-being.
• Conduct and report all types of onsite monitoring visits, including CRF reviews and source document verification.

PSI is a leading Contract Research Organisation with 30 years in the industry, offering a balance between stability and innovation. They focus on delivering quality and on-time services across a variety of therapeutic indications.