Senior Clinical Research Associate - CNS/Psychiatry - Northeast/MidAtlantic
Worldwide Clinical Trials · NJ, US
a day agoImpress employers and recruiters.
Choose from hundreds of resume examples.

Impress employers and recruiters.
Choose from hundreds of resume examples.
Tailor your resume to this Senior Clinical Research Associate - CNS/Psychiatry - Northeast/MidAtlantic role.
Rezi rewrites your resume against Worldwide Clinical Trials's job description. Free.

Tailor your resume to this Senior Clinical Research Associate - CNS/Psychiatry - Northeast/MidAtlantic role.
Rezi rewrites your resume against Worldwide Clinical Trials's job description. Free.
Don't guess if your resume is good enough.
See how it scores against the Senior Clinical Research Associate - CNS/Psychiatry - Northeast/MidAtlantic posting at Worldwide Clinical Trials — free, in seconds.

Don't guess if your resume is good enough.
See how it scores against the Senior Clinical Research Associate - CNS/Psychiatry - Northeast/MidAtlantic posting at Worldwide Clinical Trials — free, in seconds.
About the Role
As a Clinical Research Associate (CRA) at Worldwide, you will manage research activities at sites participating in clinical research projects. You will work alongside brilliant minds across diverse therapeutic areas and collaborate with top-tier colleagues. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment, offering extensive support through regulatory submissions, TMF management, and in-house CRAs. You will receive regular coaching and have a clear career path that can lead to Clinical Trial Manager roles. We offer an unparalleled experience where you can drive remarkable scientific breakthroughs.
Responsibilities
- Managing the research activities at sites participating in Worldwide’s clinical research projects
- Involved in all stages of the clinical study, including identifying potential sites, performing study start-up activities, training sites, managing site activities during study maintenance, and closing down research activities
- Conduct study initiation visits (SIVs)
- Ensuring compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
Requirements
- Candidates must reside in the MidAtlantic or Northeast United States
- Willingness to travel regionally required
Skills
- 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
Location
- MidAtlantic or Northeast United States
Work Type
- Remote
- Regional Travel
Experience Level
- 5+ years of experience as a Clinical Research Associate
Education Level
- 4-year university degree
- Nursing Degree
Salary/Compensations
- $97,000.00 - $193,000.00
Benefits
- Competitive benefits package depending on location
About the Company
- Worldwide Clinical Trials is a global, midsize CRO that pushes boundaries and innovates.
- Our mission is to work with passion and purpose every day to improve lives.
- 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.
Equal Opportunity
- We ensure pay equity and transparency and comply with all applicable labor laws.