Clinical Operations Manager
hace 2 semanas
As a Clinical Operations Manager, you will play a pivotal role in maintaining the smooth and efficient operation of our clinical services.
You will be responsible for managing and coordinating the daily activities of the operational of our clinical trials, ensuring compliance with regulatory standards, and implementing the logistic and best practices to enhance patient care.
Responsibilities:
Budget and Financial Management:
- Take ownership of country and site budgets, including the development, negotiation, and completion of Clinical Trial Research Agreements (CTRA).
- Oversee and track clinical researchrelated payments and reconcile payments at study closeout.
- Ensure compliance with financial regulations (FCPA, DPS/OFAC) and maintain financial systems.
- Collaborate with Senior Clinical Operations Manager (Sr. COM) and other roles for financial forecasting.
Clinical Trial Submissions and Approvals:
- Execute and oversee clinical trial country submissions and approvals for assigned protocols.
- Develop local language materials, including informed consents and translations.
- Interact with Institutional Review Boards (IRB) or Independent Ethics Committees (IEC) and Regulatory Authorities for protocolrelated matters.
Country Deliverables and Timelines:
- Manage country deliverables, timelines, and results for assigned protocols, ensuring compliance and quality.
- Contribute to the development of local Standard Operating Procedures (SOPs) and oversee Clinical Trial Coordinators (CTCs) as applicable.
- Coordinate with various stakeholders to obtain countryspecific submissions, budgets, and milestones.
Vendor and Process Management:
- Provide support and oversight to local vendors, ensuring compliance with requirements.
- Coordinate local processes, including supplies management, importing/exporting, filing, archiving, and insurance management.
- Maintain accurate country information in clinical and finance systems.
Regulatory and Financial Compliance:
- Ensure local regulatory and financial compliance, having a significant impact on trial commitments and objectives during study startup.
- Influence investigators, external partners, and country operations to adhere to budget targets and payment timelines.
Collaboration and Knowledge Sharing:
- Collaborate internally with various departments such as finance, regulatory affairs, and legal.
- Establish strong partnerships externally with vendors, sites, IRB/IECs, and Regulatory Authorities for submission and approvalrelated interactions.
- Contribute to initiatives and projects that add value to the business.
- Share best practices, provide training, and act as a mentor within the COM team and other Country Operations roles.
Qualifications:
- Bachelor's degree in healthcare administration, nursing, or a related field (Master's degree preferred).
- Minimum of 5 years of experience in clinical operations management and 2 years of experience in Regulatory / Finance in Clinical Research.
- Strong knowledge of healthcare regulations, compliance standards, and best practices.
- English: professional knowledge.
- Excellent leadership, communication, and interpersonal skills.
- Proven ability to lead and motivate a diverse team.
- Strong analytical and problemsolving abilities.
- Proficiency in using healthcare management software and electronic medical records systems.
Search Firm Representatives Please Read Carefully
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Hybrid
Shift:
Valid Driving License:
Hazardous Material(s):
Requisition ID:
R280006
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