What are the responsibilities and job description for the Clinical Trials Management Associate position at NexInfo Solutions, Inc.?
🚨Job Title: Clinical Trials Management Associate - I (Clinical Project Assistant)
📍 Location: Santa Monica, CA
🏢 Company: NexInfo
About NexInfo:
NexInfo is a specialized consulting firm dedicated to enhancing business processes and automation in Supply Chain and Product Lifecycle Management. With a team of industry-experienced professionals, we provide expert solutions in Business Process Design, Software Implementations, Managed Services, Staff Augmentation, and SaaS Solutions.
About the Role:
We are seeking a Clinical Trials Management Associate - I to join our team in Santa Monica, CA. This role involves providing administrative support for clinical trials, assisting with site coordination, monitoring study sites, and ensuring compliance with regulatory guidelines.
Key Responsibilities:
✔ Assist in site selection, study implementation, and coordination.
✔ Monitor routine study sites, perform data collection, and review regulatory documents.
✔ Support protocol reviews, informed consents, and study reports.
✔ Contribute to safety, interim, and final study reports.
✔ Participate in departmental initiatives and SOP development.
Qualifications:
🔹 Strong verbal, written, and interpersonal communication skills.
🔹 Familiarity with medical/scientific terminology.
🔹 Proficiency in Word, PowerPoint, and Excel.
🔹 Knowledge of FDA/EMEA regulations, ICH Guidelines, and GCPs (preferred).
🔹 Ability to travel as required.
If you’re looking for an opportunity to grow in clinical trial management and work in a dynamic environment, we’d love to hear from you!
- 📩 Apply now and be part of our innovative team at NexInfo!
Regards,
Sudheer
Senior Recruiter
NexInfo
sudheer.batha@nexinfo.com
