
Trial Management Specialist
1 day ago
We strive to improve healthcare outcomes through innovative medicines and better disease management.
Our mission is to deliver solutions across various functions, including finance, information technology, medical, clinical trials, and more. We offer a premium workspace, flexible working options, and a range of benefits.
We cater to all dimensions, ensuring inclusion of diverse ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities, and gender.
The Trial Capabilities Associate provides support for clinical trial capabilities in clinical development.
Clinical Trial Responsibilities- Initiate investigator site activities, communicate and negotiate budgets and contracts, and drive timelines aligned with company priorities.
- Meet and exceed goals for clinical trial initiation in the region of responsibility.
- Ensure site initiation and maintenance comply with local/regional requirements, data privacy, and quality standards.
- Communicate directly with sites regarding budgets and contracts activities during maintenance and close-out.
- Collect and administer financial data from contracting partners and vendors.
- Ensure finance-specific requirements are administered in budget and contract documents.
Minimum Qualification Requirements:
- Bachelor's degree in a scientific, health-related, engineering, economics, or project management field.
- Two years' clinical research experience (CRO, sponsor, or healthcare service provider) or relevant budget and contract negotiation experience preferred.
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