Director, Oncology Trials BD & Delivery (Remote)

Massive Bio, Inc.; South Carolina; Remoto; USD 180.000 - 230.000; Tempo pieno

Descrizione del lavoro

Massive Bio, Inc. is seeking a Director of Business Development & Client Delivery to drive sponsor relationships for SentinelAgent™, our oncology trial monitoring platform.

You will own end-to-end engagement from initial pilot to multi-study agreements, ensuring compliant close-out and value delivery across US sites. You will combine business development with product feedback, coordinating with QA and regulatory teams to align with FDA/EMA expectations.

Competenze

• Must have 7+ years in US clinical research with hands-on data-side experience at a site, SMO or CRO.
• Experience with CRF entry and SDV workflows in US EDC systems.
• Sponsor-facing business development and account management experience with pilots to contracts.
• Close-out visits and essential-record reconciliation experience.
• Strong knowledge of FDA/EMA regulatory expectations and clinical trial regulation.

Mansioni

• Lead business development and client delivery, managing sponsor relationships end-to-end.
• Translate sponsor needs into costed pilots and multi-study agreements.
• Draft statements of work under master agreements and manage papering of engagements.
• Price services within a published rate card and obtain approvals for exceptions.
• Ensure compliant close-out deliverables including data, safety, and records.
• Coordinate with QA/Regulatory to map processes to FDA/EMA requirements.

Conoscenze

US clinical research

CRF entry/SDV workflows

Sponsor-facing business development

Close-out/reconciliation

Regulatory compliance knowledge

Formazione

Bachelor's degree in life sciences

Strumenti

Medidata Rave

Oracle Clinical One

InForm

Veeva Vault EDC

Descrizione del lavoro

Massive Bio, Inc. is seeking a Director of Business Development & Client Delivery to drive sponsor relationships for SentinelAgent™, our oncology trial monitoring platform.

You will own end-to-end engagement from initial pilot to multi-study agreements, ensuring compliant close-out and value delivery across US sites. You will combine business development with product feedback, coordinating with QA and regulatory teams to align with FDA/EMA expectations.