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Clinical Study Associate - Contract - Basking Ridge, NJ

À±½·ÊÓƵ is partnering with a biotech company to recruit a Clinical Study Associate to support the planning and execution of clinical studies.

Primary Responsibilities:

The successful candidate will work closely with a Senior Manager in Clinical Operations to ensure studies adhere to protocols and regulatory guidelines. Key responsibilities include providing administrative support to study teams and coordinating with Contract Research Organizations (CROs) and other vendors to ensure compliance.

Skills & Requirements:

• Strong organizational and communication skills.
• Ability to work collaboratively with study teams and external partners.
• Familiarity with clinical study protocols and regulatory guidelines.

The Clinical Study Associate's responsibilities will be:

• Assist in the planning and execution of clinical studies.
• Provide clinical administrative support to study teams.
• Interact with CROs and vendors to monitor study compliance.
• Ensure adherence to protocols, GCPs, SOPs, FDA regulations, and ICH guidelines.

If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at j.jones@proclinical.com

À±½·ÊÓƵ is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

À±½·ÊÓƵ Staffing is an equal opportunity employer.