Contract Clinical Project Manager

October 7, 2024

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D2V Clinical

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D2V Clinical is a full-service global Contract Research Organization (CRO) specializing in the development of oncology, hematology, and acute/chronic diseases. The company partners with biopharmaceutical sponsors to deliver in-depth clinical development insights and operational solutions. D2V Clinical focuses on creating investor value by leveraging extensive experience in early clinical development, regulatory affairs, and project management. With a robust network of clinical sites and patient recruitment strategies, D2V Clinical is dedicated to expediting drug signal detection and advancing therapeutic programs in the oncology sector.

51 - 200 employees

Founded 2019

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

📋 Description

• This is a remote position. • We are recruiting for a Contract Clinical Project Manager to help support our clients throughout the various phases of our projects. • Dose2Value Clinical (D2V Clinical) is a full-service global CRO addressing the challenges of early-phase studies faced by biotech companies. • The Clinical Project Manager (CPM) is responsible for the management of all aspects of Clinical Trial Team activities for assigned project(s). • The CPM, in concert with the Head of Clinical Operations is accountable for achieving successful delivery of clinical team activities at the project level by meeting company and regulatory requirements according to time, quality/scope and budget constraints. • Proactively manage project level operational aspects of Clinical Trial Team (CTT) including management of trial timeline, budget, resources and vendors. • Provide efficient updates on trial progress to the Clinical Program Director (CPD) and/or Senior Director of Clinical Operations (DCO), with respect to vendor selection, project plans, trial budget and timeline management, quality standards and risk mitigation.

🎯 Requirements

• Bachelor’s degree, and a minimum four (4) years of clinical operations experience; with increasing levels of responsibility, in the Pharmaceutical, Biotechnology, Medical Device or CRO industry is required or an equivalent combination of education and experience. • Proficiency in Microsoft Office Suite. • Working knowledge of various clinical systems (e.g., electronic data capture [EDC]). • Knowledge of guidelines, ICH-GCP and other applicable local and international industry regulations. • Attention to detail, highly organized, and the ability to multitask and prioritize in a face-paced, highly interactive environment. • Self-starter and independent learning ability. • Ability to work independently and in a team environment. • Strong communication skills (verbal and written) to express complex ideas to multidisciplinary teams and/or management. • Up to 20% travel may be required domestically.

🏖️ Benefits

• This is an independent contractor role and is not eligible for employee benefits