Clinical Project Manager (FSP) at Parexel

, , China -

Full Time

Start Date

Immediate

Expiry Date

22 Dec, 25

Salary

0.0

Posted On

23 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Delivery Skills, Interpersonal Skills, Leadership Skills, Process Competency, SOP Competency, GCP Competency, Drug Regulations, Computer Skills, Fluent English, Training Delivery

Industry

Biotechnology Research

Description

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities: Study Management Forecast timelines, budget & FTE resource ( if applicable). Take a key leadership role in the management of studies’ timeline, quality, cost. Ensures all activities must be in compliance with SOPs, applicable policies and related standards, and in line with GxP, local laws and regulations. Monthly track and manage the agreed studies’ timelines, budget and resource, highlight significant variance and take appropriate actions to get studies on track. Update study information into VCV, Evidence Connect system, Medical Tracking system, and update to global & regional team to ensure up-to-date information captured . Timely update projects information to the Brand Team. Review and approve project relevant documents. Lead preparation and delivery of study documents (e.g. Protocols/amendments, ICF, CRF, studies’ related plans and forms, etc.) Prepare and lead investigator and monitor meeting. Ensure AEs/SAE reporting according to GCP and regulation. Plan and lead activities associated with study level Quality Control plan. Develop & manage contingency risk plans to assure timely delivery to quality, budget, and time and escalate issues to stakeholders as appropriate. Provide operational support to the ESR investigators to ensure the on time delivery of ESR Compliance with Parexel standards Comply with required training curriculum. Complete timesheets accurately as required. Submit expense reports as required. Update CV as required. Maintain a working knowledge of and comply with Parexel processes, ICHGCPs and other applicable requirements. Skills: Advanced level project delivery skills, including experience of study start up, ongoing phase and study close out Strong interpersonal skills, with the ability to work effectively with others at all levels of the organization Leadership skills Excellent process, SOP, GCP and company policy competency, and drug regulations • Good computer skills in Microsoft and other software. Fluent in both oral and written English Proven ability to deliver training Knowledge and Experience: Minimum 2–3-year experience of project management experience. Prior experience not only as a clinical management staff, but responsible for training/ quality assurance/quality control/ procedural document development Read, write, and speak fluent English; fluent in host country language required. Education: Bachelor’s or higher degree in Science, Medical or Pharmaceutical Background Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.

Responsibilities

The Clinical Project Manager is responsible for managing study timelines, quality, and costs while ensuring compliance with relevant regulations. They will lead the preparation and delivery of study documents and manage operational support for investigators.