TruMinds Clinical
Website:
trumindsclinical.com
Job details:
Company Description: TruMinds Clinical is a global Functional Service Provider (FSP), clinical staffing, and CRO partner serving pharmaceutical, biotechnology, medical device, and healthcare companies, and CROs across the USA and internationally. The organisation delivers customized life sciences services, processes, and reporting across all therapeutic areas, supporting monitoring, clinical trial management, drug safety, data management, and statistical programming. TruMinds Clinical provides flexible workforce and project-based outsourcing solutions, partnering with clients of all sizes, including several of the top 10 pharmaceutical companies and small to midsize biotech organizations. With 25 years of experience in clinical research and trial execution from Phase I–IV, the company manages global clinical trials across a broad range of indications. TruMinds Clinical is highly result-oriented, offering efficient, cost-effective clinical trial services in the USA, Canada, the UK, and India.
Role Description The Senior Clinical Project Manager is a full-time, remote role responsible for leading and overseeing complex clinical trials from start-up through closeout. This role coordinates cross-functional teams, manages timelines, budgets, and deliverables, and ensures trials are conducted in compliance with protocols, regulatory requirements, and quality standards. Daily activities include planning and tracking project milestones, supervising clinical operations activities, managing vendor and site performance, and identifying and mitigating project risks. The Senior Clinical Project Manager will collaborate closely with sponsors and internal stakeholders, prepare project status reports, and drive continuous process improvement across assigned studies. This position also mentors project team members and contributes to the development of best practices for trial management within TruMinds Clinical.
Qualifications
- Strong experience in Trial Management and Clinical Operations, demonstrating the ability to lead global Phase I–IV clinical studies.
- Proven Project Management skills, including planning, resource allocation, risk management, and budget oversight.
- Solid background in clinical Research and protocol execution, with expertise in interpreting and implementing study protocols.
- In-depth knowledge of ICH-GCP, FDA and other global regulatory guidelines, and clinical quality standards.
- Bachelor’s or advanced degree in life sciences, pharmacy, nursing, or a related field.
- Several years of progressive experience in clinical project management within pharma, biotech, or CRO environments.
- Excellent communication, stakeholder management, and leadership skills, with the ability to work effectively in remote, cross-functional teams.
- Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC), and common project management tools.
- Ability to work independently, manage multiple concurrent projects, and adapt to changing priorities in a global setting.
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