Clinical Development Project Manager

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee the execution of Clinical Development projects, ensuring that milestones are met on schedule, within the defined scope, and in accordance with clinical and organizational priorities.

• Create and maintain comprehensive project plans, dependency maps, and risk management registers.

• Actively address and mitigate risks related to delivery, data, and validation throughout dry lab workflows.

• Facilitate collaboration among cross-functional teams in bioinformatics, software engineering, clinical operations, and product development.

• Propel project execution, tackle obstacles, and guarantee accountability for all deliverables.

• Convert intricate analytical and computational requirements into clear and actionable project deliverables.

• Aid in the development of scalable and compliant genomic analysis and reporting processes.

• Track and evaluate project performance metrics, including adherence to timelines, risk patterns, and validation readiness.

• Provide project updates, highlight risks, and summarize outcomes to program leadership through concise, data-driven communications.

• Assist with documentation, audits, and validation tasks to maintain compliance with regulatory standards, quality, and data governance.

• Carry out additional responsibilities as required to support team and organizational goals.

• Adhere to company policies, procedures, and relevant regulatory mandates.

⛳️ Requirements

• Bachelor’s degree in Life Sciences, Genetics, Molecular Biology, Public Health, Healthcare Administration, Clinical Research, or a related discipline.

• A minimum of 4 years of pertinent experience in clinical lab operations, development and research, diagnostics, biotechnology, healthcare, or similar fields.

• At least 2 years of experience managing cross-functional projects with responsibility for timelines and deliverables.

• Proven ability to handle multiple technically complex projects concurrently.

• Extensive experience in managing cross-functional teams, including bioinformatics scientists, software engineers, analysts, and clinical stakeholders.

• Demonstrated experience with data pipelines, analytical workflows, or laboratory informatics platforms.

• In-depth understanding of technical dependencies, system integrations, and validation aspects in regulated environments.

• Exceptional communication, organizational, and leadership abilities.

• Strong interpersonal skills, negotiation capabilities, and proficiency in facilitating technical meetings.

• Proven ability to navigate teams through ambiguity, shifting technical requirements, and data-driven decision-making.

• Capability to collaborate effectively with stakeholders at all levels, including both technical and non-technical audiences.

• Strong analytical and problem-solving skills, with a focus on identifying and mitigating technical and delivery risks.

• Keen attention to detail, data precision, and process diligence.

• Commitment to continuous improvement and operational excellence.

• An equivalent combination of education and experience may be acceptable.

• Master’s degree in life sciences or a related field is preferred.

• Project management certifications (PMP or equivalent) are preferred.

🏝️ Benefits

• May require occasional travel to conferences, partner sites, healthcare institutions, or company meetings.