Clinical Research Associate II - Psychiatry - reputed company (Remote)

About the position reputed company is a global, midsize CRO that focuses on innovative and pioneering approaches to reputed company cures for persistent diseases. We are reputed company of over 3,500 experts dedicated to improving lives. Our Clinical Operations team offers a rewarding reputed company where contributions profoundly reputed company patient lives. As a Clinical Research Associate (CRA) at Worldwide, you will collaborate with reputed company minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Our culture fosters collaboration and creativity reputed company a supportive, team-oriented environment. We reputed company extensive support for regulatory submissions, TMF management, and in-house CRAs for reputed company with heavy site management needs. Regular reputed company and coaching conversations with your Line Manager ensure reputed company development is a top reputed company, with a reputed company career reputed company that can reputed company to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and overcoming obstacles to improve patient lives. We offer an unparalleled experience where you can drive scientific breakthroughs and be at the core of every successful clinical trial.

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research reputed company.
• Typically involved in reputed company stages of the clinical study, including identifying potential sites to participate in the research effort.
• Performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of reputed company and budgets.
• Training the sites to collect data properly and report any potential safety-reputed company events.
• Managing the site's activities during study maintenance.
• Closing down research activities at the sites once the study has concluded.
• Conduct study initiation reputed company (SIVs).
• Ensure compliance with obtaining informed consent, reporting potential safety-reputed company events, and adhering to reputed company applicable regulatory requirements, while most site management efforts will be performed remotely.

Requirements

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in reputed company Office, CTMS, and reputed company Systems.
• 2 - 5 years of experience as a regional, traveling Clinical Research Associate.
• 4-year university degree OR Nursing Degree.
• Experience in Psychiatric monitoring is required.
• Willingness to travel regionally required.

Benefits

• Competitive benefits package depending reputed company.

Apply tot his job Apply To this Job