Senior Clinical Research Associate - CNS/Psychiatry - Central U.S.

Worldwide Clinical Trials • Research Triangle Park, NC

2d • Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that is looking for a Senior Clinical Research Associate with expertise in CNS/Psychiatry to join their team. The company is committed to changing the way the world experiences CROs by taking pioneering, creative approaches to cure persistent diseases. They foster a diverse and inclusive environment where professionals from all backgrounds can thrive and contribute to improving patients' lives. The Clinical Operations team at Worldwide offers a rewarding journey where contributions have a profound impact on patients' lives. CRAs work alongside brilliant minds across diverse therapeutic areas and collaborate with top-tier colleagues. The role provides extensive support through regulatory submissions, TMF management, and in-house CRAs. Professional development is a priority, with regular touchpoints and coaching from Line Managers, and a clear career path that can lead to Clinical Trial Manager roles. The Executive Leadership team is accessible and committed to advancing science and overcoming obstacles.

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 Microsoft Office, CTMS, and EDC Systems.
• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree OR Nursing Degree.
• Experience in CNS/Neurology is required.
• Psychiatry experience is strongly preferred.
• Candidates must reside in the Central U.S.
• Willingness to travel regionally required.

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
• Typically involved in all stages of the clinical study, including identifying potential sites, performing study start-up activities (collecting regulatory documents, supporting contract and budget negotiation), training sites on data collection and safety reporting, managing site activities during study maintenance, and closing down research activities at sites.
• Conduct study initiation visits (SIVs).
• Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements, with most site management efforts performed remotely.

Benefits

• We believe everyone plays an important role in making a world of difference for patients and their caregivers.
• From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed.
• We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
• We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.
• We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Associate degree