Operations Manager, Clinical Research

Scope of Responsibilities

• Affirms feasibility of research protocols by reviewing clinical, operational, and resource requirements and recommending suitable trials for the medical institution.
• Maintains oversight of budget negotiations and study activation timelines to ensure timely site readiness.
• Manages the team of (Lead) Study Coordinators, ensuring their work meets quality standards through monitoring and follow-up of various operational tools.
• Promotes process improvement and standardization of clinical trial operations in alignment with ICH GCP, regulatory requirements, and internal policies, by contributing to the development of operational guidelines, templates, and procedures.
• Fosters a work culture that emphasizes transparency, accountability, and continuous learning.

Qualifications

• Associate degree in life sciences or similar field.
• Business Management degree or certification is a plus.
• Certified in ICH GCP training.
• Minimum 5 years of clinical research experience, preferably in a leadership role at a clinical research facility or network.
• Knowledgeable and experienced in the entire lifecycle of clinical research activities, from pre-award through close-out.
• Fluent in English.
• Proficient in MS Office.
• Valid Category B driver’s license.
• Exceptional communication and management skills.
• Strong problem-solving and result-oriented abilities.
• Accountability and team leadership skills.