What are the responsibilities and job description for the Clinical Operations Study Associate II position at Integrated Resources, Inc?
Job Title: Clinical Operations Study Associate IIJob Location: Cambridge, MA (Remote)Duration: 7 Months Pay Rate: $63.33/hr. on w2 Duties:Support the Clinical Operations Study Leader and team in managing and overseeing clinical trials. Reports to an Associate Director of Clinical Operations (or above).ResponsibilitiesAssist in day-to-day trial execution: site start-up, enrollment, monitoring, and data flow.Prepare study documents (consent forms, site instructions, manuals, pharmacy binders).Track essential documents in TMF; review site documents for accuracy.Monitor patient status and sample collection; manage lab schedules and vendor coordination.Liaise with CROs and sites for sample handling and reporting.Review monitoring reports, data queries, and site performance metrics.Attend site visits and co-monitor with CRO.Ensure data quality and resolve eligibility/protocol deviation issues.Support investigator/vendor meetings and feasibility assessments.Review site contracts and budgets; coordinate third-party vendor activities.Education:Qualifications:Bachelor’s degree in science or higher.Skills:Resourceful and flexible in dynamic environments.Highly organized with strong multi-tasking skills.Collaborative team player.Self-Starter & Results Driven: Takes initiative, identifies opportunities, and drives deliverables with minimal supervision.3 years in pharma, CRO, or clinical research environment.Knowledge of GCP and SOPs; understanding of study phases.Proficient in Word, Excel, PowerPoint; database management basics.Strong verbal and written communication skills.PreferredMedical/scientific experience in clinical research.Experience in monitoring, study coordination, or data handling#sczr2
Salary : $63