Study Startup Lead at PSI CRO

Shanghai, Shanghai, China -

Full Time

Start Date

Immediate

Expiry Date

08 Feb, 26

Salary

0.0

Posted On

10 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Study Startup, Feasibility Research, Site Identification, eTMF Maintenance, Site Agreement Negotiation, Budget Negotiation, Study-Specific Translations, Project Communication, Site Activation Progress, Site Selection Visits, Field Training, Communication Skills, Organizational Skills, Leadership Skills, Mentoring Skills, Relationship Building

Industry

Pharmaceutical Manufacturing

Description

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 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description Take your career to the next level and be involved in study startup processes in China. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Office-Based: Shanghai You will: Leads all study startup activities/processes with local project teams. In the absence of stand-alone feasibility function, leads activities in feasibility research and site identification process. Oversees electronic Trial Master File (eTMF) maintenance during startup phase. Leads activities on negotiation of site agreement and/or budget to ensure alignment to the site activation plan. Reviews study-specific translations. Identifies project-specific issues and escalates to all functions concerned as outlined in the Project Communication Plan. Supervises preparation and/or submission of the study dossiers to sites, to the competent authorities, IRBs/IECs, etc. Reviews IP-REDs packages. Oversees and reports on the site activation progress of the clinical sites. If qualified, conducts site selection visits and/or functions as a field trainer for SSVs. Qualifications Bachelor's or above degree in Pharmaceutical, Medical, Nursing and Life Sciences relevant major. At least 6 years of full-scope Study Startup experience in the country/region. Well-developed communication and organizational skills. Ability to negotiate and build relationships at all levels. Leadership, mentoring, and organizational skills Additional Information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Responsibilities

Leads all study startup activities and ensures smooth and timely initiation of clinical projects. Oversees site agreement negotiations and maintains the electronic Trial Master File during the startup phase.