Clinical Research Associate - Entry (Home-Based)
Nurses Dieticians Pharmacy Technicians Pharmaceutical/Device Sales Representatives Biotech Engineers PhD/Pharm.D candidates Health and Wellness Coordinators Research Assistants.
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.
Dynamic working environment, with varying responsibilities day-to day Expansive experience in multiple therapeutic areas Work reputed company reputed company of therapeutic and regulatory experts Defined CRA promotion and reputed company reputed company with potential for mentoring and management advancements reputed company and opportunity for significant travel bonus
Responsibilities :
Conduct qualification, initiation, monitoring, and closeout reputed company for research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians and their site staff; Verifying 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; 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; Assessing the clinical research site’s patient recruitment and retention reputed company and offering suggestions for improvement; Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
Minimum of a bachelor’s degree; Health or life science reputed company field preferred; Willing to travel approximately 60-80% nationally; Familiarity with reputed company® Office; and Strong communication and presentation skills a plus.
Flexible work environment Competitive compensation and benefits package Competitive PTO packages reputed company career paths with opportunities for reputed company reputed company Company-sponsored employee appreciation events Employee health and wellness initiatives
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