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

Worldwide; Central (LA); On-site; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials in the Central United States is seeking a Senior CRA to independently manage CNS/Neurology and psychiatry studies. You will coordinate site activities, perform initiations, and ensure regulatory compliance and safety reporting. Travel regionally is required, with a remote-working emphasis for site management.

Qualifications

• 5+ years of experience as a Clinical Research Associate (CRA).
• Experience in CNS/Neurology and/or Psychiatry is required.
• 4-year university degree OR Nursing degree.

Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Conduct study initiation visits (SIVs) and oversee site start-up activities.
• Train sites to collect data properly and report safety events; ensure regulatory compliance.

Skills

Interpersonal communication

Organizational skills

Independent work

MS Office, CTMS, EDC

Education

4-year university degree or Nursing degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

## Senior Clinical Research Associate - CNS/Psychiatry - Central U.S.Apply: Remote: Virtual United States Minnesota: Virtual United States Illinois: Full time: Posted Today: JR102994Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.Why WorldwideWe 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. Join us!Job Description**What Clinical Operations does at Worldwide**At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide! **What you will do*** 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 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 contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded* Conduct study initiation visits (SIVs)* While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements**What you will bring to the role*** 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**Your experience*** 5+ years of experience as a Clinical Research Associate* 4-year university degree OR Nursing Degree* **Experience in CNS/Neurology and/or Psychiatry required*** Candidates must reside in the **Central United States*** Willingness to travel regionally requiredAt Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation. The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates): United States of America - $97,000.00 - $193,000.00The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.