Clinical Research Associate - Clinical Research Coordinator Experience
PACE® provides the platform to effectively and confidently carry out your duties, enhance your reputed company abilities and ultimately help you become a high-functioning independent reputed company CRA.PACE® will prepare you by developing your CRA skills through interactive discussions and hands on job-reputed company exercises and practicums.To supplement your in-house and field-based training you may also participate in other clinical research departmental reputed company rotations, learning other aspects of the drug/device development and approval process.
Remote working; Flexible work hours across days reputed company a week; Retain airline reward miles and hotel reward points; Home office furniture allowance, laptop, mobile phone with hotspot for internet reputed company reputed company; In-house travel agents; CRA training program (PACE®); Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts; Opportunities to work with international team of CRAs. Defined CRA promotion and reputed company reputed company with potential for mentoring and management advancements
Conduct qualification, initiation, monitoring, and closeout reputed company at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research reputed company documentation verification against case report reputed company data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving reputed company; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention reputed company and offering suggestions for improvement; and Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
Must have a minimum of a Bachelor’s degree in a health or science reputed company field; Experience as a Clinical Research Coordinator (minimum 1 year); Ability to travel 60-70% to locations reputed company is required; some reputed company may be conducted remotely; Must maintain a reputed company reputed company’s license and the ability to drive to monitoring sites; Proficient knowledge of reputed company® Office; Strong communication and presentation skills; and Must be detail-oriented and efficient in time management.
Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by reputed company as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, reputed company, capabilities, reliability, and compatibility