Senior Clinical Research Associate
Core
Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical research projects and study submissions
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Onsite monitoring, Source document verification, Query resolution, Site management, Regulatory document preparation, Feasibility research, Quality control, Phase I-III trial experience, Oncology trial monitoring, Radiopharmaceuticals knowledge, Breast cancer trial monitoring, GI studies monitoring (IBD, Chron's, UC)
Preferred skills
Radiopharmaceuticals experience, Breast cancer trial experience, GI studies experience
Technologies
MS Office
Responsibilities
Conduct and report onsite monitoring visits, Perform CRF review and source document verification, Manage site communication and relationships, Supervise study activities and timelines on a country level, Participate in study startup and feasibility research, Support regulatory team in preparing submission documents
Seniority
Senior, hands-on IC
