• Associate Scientist, Clinical Operations

    Insight Global (Florham Park, NJ)


    Job Description

    A large CPG client of ours is looking for someone to assist with managing clinical supply operations to ensure accurate labeling, storage, and accountability of all materials. Key duties include coordinating supply ordering, shipping, and timely delivery to study sites, as well as overseeing the return management of unused supplies in compliance with regulations. The position requires maintaining precise documentation aligned with SOPs, GMP, and quality standards, while fostering strong relationships with internal teams and external partners. Additional responsibilities include reviewing study-related documents and performing other tasks as needed to support clinical operations. This will start as a 3 month contract with possibility of extension.

     

    We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

    Skills and Requirements

    •Associate’s or related degree in Life Sciences, Health Sciences or related field.

    •Minimum of 1-3 years of lab/ R&D experience

    •Excellent written and verbal communication skills, interpersonal and organization skills are a must.

    •Experience effectively working in cross-functional teams.

    •Team player with the ability to work independently to accomplish objectives within the timelines established

    •Ability to work effectively in a fast-paced environment

    •Knowledge of GMP and ICH requirements Previous CPG experience