Description

In this pivotal role you will oversee global and regional Phase I‑IV trials in Oncology, Rare Diseases, or CNS, ensuring delivery within agreed timelines, scope, cost, and quality. You will be involved in every study stage—from proposal strategy and costing to bid defence and full‑cycle execution—while managing client relationships, project teams, and budgets.

You will collaborate with cross‑functional internal and external stakeholders, driving quality and coordinating the study team. The company offers a high‑energy, dedicated, and collaborative environment where detail‑oriented professionals thrive in dynamic settings and can take charge of extraordinary work.

Key responsibilities include independently leading clinical projects, serving as the primary client liaison, and handling all aspects of trial management across functional areas such as data management, safety, clinical monitoring, and biostatistics. You will prepare project status updates, review protocols and study documentation, and contribute to efficient trial execution.

• Lead full‑service clinical trials (Phase I‑IV) globally in Oncology, Rare Diseases, or CNS.
• Manage project scope, timelines, budget, and quality across all functional departments.
• Serve as primary client liaison, delivering proposals, presentations, and ongoing communication.
• Coordinate cross‑functional teams, including data management, safety, medical monitoring, and biostatistics.
• Prepare and review protocols, informed consents, site contracts, and budgets; provide status updates and performance metrics.

Requirements

Precision for Medicine (CRO) seeks an experienced full‑service Project Manager with a focus on oncology clinical trials. The ideal candidate is passionate about improving patient health worldwide and takes a consultative approach to trial management, acting as a valuable partner in operational delivery.

Applicants must hold a life‑science degree or equivalent, have 5‑7 years of industry experience (including at least 4 years in full‑service project management within a CRO), and possess proven oncology trial experience. Strong knowledge of GCP/ICH guidelines, excellent English communication, presentation skills, and proficiency with MS Office, MS Project, CTMS, eTMF, EDC, and IXRS are required. The organization promotes a supportive, collaborative culture with work‑life balance and equal‑opportunity employment.

• Require a life‑science degree (or equivalent) with 5‑7 years industry experience, including 4 years as a full‑service Project Manager in a CRO.
• Demonstrated oncology trial management experience and strong knowledge of GCP/ICH guidelines.
• Excellent English communication, presentation, and MS Office/Project/CTMS/EDC software skills.
• Ability to travel domestically and internationally, including overnight stays.

Benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance