What are the responsibilities and job description for the Clinical Trials Management Associate – I position at Omiz Staffing Solutions (OSS)?
We're Hiring! Clinical Trials Management Associate – I 🚨
One of our Biopharmaceutical customers is seeking a Clinical Trials Management Associate to join their team and contribute to groundbreaking advancements in clinical research. This is an exciting opportunity to play a vital role in site selection, study implementation, and ongoing coordination of clinical trials.
Role : Clinical Trials Management Associate – I
Location : Santa Monica, CA
Pay Rate : $45 - $50 / hour (W2)
Contract Duration : 6 to 7 months (possible extension)
Key Responsibilities :
- Provide administrative support in site selection, study setup, and ongoing site coordination (directly or via CROs).
- Monitor study sites to ensure compliance with protocols, regulatory requirements, SOPs, and Monitoring Plans.
- Assist in reviewing protocols, informed consents, case report forms, and clinical study reports.
- Support the preparation of investigator brochures, safety reports, and regulatory documents.
- Resolve routine monitoring issues and contribute to data integrity and quality.
- Participate in departmental initiatives and SOP development.
- Travel is required.
What We're Looking For :
Strong verbal, written, and interpersonal communication skills.
Familiarity with medical / scientific terminology.
Proficiency in Microsoft Word, PowerPoint, and Excel.
Knowledge of FDA / EMEA regulations, ICH Guidelines, and GCPs (preferred).
Ability to work collaboratively and contribute to strategic initiatives.
Apply today and be part of a team dedicated to advancing global health!
Interested? Apply now or DM us for more details!
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Salary : $45 - $50