The Proposal Analyst is responsible for analyzing RFPs and preparing high-quality proposals and budgets in collaboration with internal stakeholders. They manage the electronic archive of proposals and implement pricing strategies to drive business growth.
The eTMF Specialist is responsible for maintaining the electronic Trial Master File, ensuring accurate filing, and performing quality reviews of study documentation. They act as the primary contact for study teams regarding archiving and ensure the eTMF remains inspection-ready.
Identify and engage potential pharma and biotech clients through outreach and research to expand the global client network in the APAC region. Coordinate meetings between clients and experts while maintaining CRM data and nurturing long-term partnerships.
As a Clinical Research Associate, you will coordinate and oversee the execution of clinical studies according to protocols and regulations. You will perform site monitoring visits, interact with trial teams, and manage study documentation.
Identify and engage potential clients through various outreach methods and coordinate meetings between clients and OPIS experts. Maintain CRM data and nurture client relationships to support long-term partnerships.
