You will lead statistical input for clinical study design, develop SAPs, and perform sample size calculations. Additionally, you will deliver high-quality statistical outputs using SAS and collaborate cross-functionally with data management and study teams.
The Proposal Analyst is responsible for analyzing RFPs and preparing high-quality, competitive budget proposals in collaboration with internal stakeholders. They must ensure compliance with privacy regulations while maintaining accurate electronic archives and optimizing proposal processes.
You will identify and nurture new business opportunities within the life sciences sector by connecting with key decision-makers in pharmaceutical and biotechnology companies. Additionally, you will manage CRM data, conduct outreach via phone and email, and organize meetings between potential clients and the internal team.
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.
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.
