[Hiring] Regional Project Lead @PSI CRO

Remote Full-time
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,000 driven, dedicated and passionate individuals. We work on the front-line of medical science, changing lives, and bringing new medicines to those who need them. If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. Job Description The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level. • Ensures planning, implementation, and management of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents (e.g., PSI QSDs or Sponsor QMS documents) • Acts as primary or secondary project management contact for the project team and PSI support services in designated countries • Performs study status review and progress reporting (if delegated by the Project Manager) • Collects and reports project status updates for designated regions, both internally and externally • Develops and updates project planning documents, essential study documents and project manuals/ instructions • Manages and reports on Key Performance Indicators (KPIs) for designated countries and clinical project team members • Ensures that the project timelines and subject enrollment targets are met in designated countries • Coordinates maintenance of study-specific and corporate tracking systems • Coordinates site contractual startup and budget negotiations • Establishes communication lines within the project team and supervises clinical project team members’ performance • Identifies, escalates and resolves resourcing and performance issues • Conducts and supervises therapeutic area training of the project team (if delegated by the Project Manager) • Prepares presentations and conducts training of Investigators • Ensures team compliance with project-specific training matrix • Performs field training of Monitors tailored to the project needs • Supervises preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits • Oversees investigator and site payments, as well as CRF data retrieval/ upload and monitoring and the query resolution process • Supervises project team preparation for study audits/ inspections and resolution of audit/ inspection findings • Coordinates conduct of supervised monitoring visits • Reviews site visit reports and ensures monitoring and reporting standards are met • Coordinates preparation of initial and follow-up Regulatory and Ethics Committee submissions and notifications • Oversees the safety information flow and participates in feasibility research • Reviews/ approves project related expenses and timesheets (if delegated by the Project Manager) Qualifications • College/University degree in Life Sciences or an equivalent combination of education, training & experience • Significant experience in Clinical Research and site monitoring • Experience as a Study Manager or Lead with the ability to supervise project activities as a Regional Lead or equivalent • Experience in Oncology is preferred. • Full working proficiency in English • Proficiency in MS Office applications, including MS Project • Communication, presentation and customer-service skills • Ability to negotiate and build relationships at all levels • Team-building, leadership and organizational skills Additional Information Advance your career in clinical research and lead challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first! You will get hands-on involvement in every aspect of the study. For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future. Apply tot his job Apply tot his job
Apply Now →

Similar Jobs

Project Leadership, Biotech, Clinical trials','Oncology','Home Based','Future Needs

Remote Full-time

Remote .NET Developer (Part-time)

Remote Full-time

Senior Software Engineer - C# (Multiple Positions Available)

Remote Full-time

Executive Partner – CIO/CTO Advisory, Life Sciences

Remote Full-time

C#/.NET Desktop Developer | Remote But Must Be Located In Montana

Remote Full-time

Software Engineer (C#)

Remote Full-time

Trainer - Curriculum Developer Remote, US

Remote Full-time

[Remote] Curriculum Content Developer

Remote Full-time

Remote Crypto Finance Analyst for Global Portfolio

Remote Full-time

[Remote] Crypto Investment Analyst

Remote Full-time

Vascular Access Nurse Consultant - PICC RN

Remote Full-time

Experienced Full-time Data Entry Coordinator – Entry Level Remote Position for Detail-Oriented Professionals with Opportunities for Growth and Development at blithequark

Remote Full-time

Experienced Data Entry Clerk for Remote Work Opportunity at blithequark

Remote Full-time

HR Recruiter

Remote Full-time

E-Filing Specialist (FULLY REMOTE)

Remote Full-time

IoT Engineer

Remote Full-time

**Remote Customer Experience, Marketing & IT Support Specialist – Join Coca‑Cola’s Global Virtual Workforce and Shape the Future of Refreshment from Home**

Remote Full-time

Hybrid Police Communication Specialist (Police Dispatcher) - Ft. Worth, TX (Fort Worth, TX, US, 76131)

Remote Full-time

Remote Data Entry Clerk & Virtual Assistant - Flexible Part-Time Opportunity with Competitive Hourly Rate up to $21/hr at blithequark

Remote Full-time

Experienced Remote Data Entry Specialist - Join blithequark's Flexible and Rewarding Career Path

Remote Full-time
← Back to Home