PSI CRO

Global CRO delivering on-time patient enrollment

Therapeutic Area - Associate, Director

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeShanghai, ChinaNo salary listed

About the Job

Requirements

At least 10 years of experience in a clinical research CRO or pharmaceutical environment.
MD or Pharmacy education background, specific in Oncology.
Knowledge or experience expanding local clinical development activities from China to overseas, especially Europe and/or the United States.
Must be comfortable travelling to other cities in China for meetings and conferences.
Must possess business-level English to communicate with the global department.

Responsibilities

Participate in indication-specific strategy planning and implementation across the assigned therapeutic area.
Compile and deliver presentations on lessons learned.
Mentor, train, and assist department staff in developed strategies and best practices within the assigned therapeutic area.
Participate in external Executive Oversight Meetings.
Join the Core Project Team within the designated therapeutic area to advise on therapeutic strategy.
Participate in the evaluation and selection of investigators and sites.
Participate in investigator meetings and various team meetings.
Identify key project-level risks and escalate them to senior management.
Review essential study documents.
Assess team members’ performance during bid defenses and provide feedback.
Attend and follow up on internal and external study audits.
Attend conferences in the therapeutic area and review supporting literature.
Make bidding recommendations based on reviews of feasibility evaluations and requests for proposals.
Assist and mentor the bid team in bid-defense processes, coach the team on strategy and key therapeutic-area elements, participate in bid-defense preparation, and attend bid-defense meetings.
Contribute to developing PSI’s global therapeutic strategy in line with its indication-specific portfolio.
Assist in developing and maintaining an indication-specific key opinion leader and specialist network.
Build working relationships and maintain communication with business stakeholders.

Job Description

1. Therapeutic Oversight

Is involved in indication-specific strategy planning and implementation across the assigned therapeutic area.
Compiles and delivers presentations on lessons learned.
Mentors, trains, and assists department staff in developed strategies and best practices within their assigned therapeutic area.
Participates in external Executive Oversight Meetings.
Joins the Core Project Team within the designated therapeutic area to advise on the therapeutic strategy.
Participates in the evaluation and selection of investigators and sites.
Participates in investigator meetings and various team meetings.
Identifies key project-level risks and escalates to senior management.
Reviews essential study documents.
Assesses performance of team members during bid defenses and provides feedback.
Attends and follows up on internal and external study audits.
Attends conferences in the therapeutic area, and reviews supporting literature.

2. Business Development

Makes recommendations for bidding based on review of feasibility evaluations and RFPs.
Assists and mentors the bid team in the bid defense processes and coaches team in strategy and key therapeutic area elements, takes part in bid defense preparation, and attends bid defense meetings.
Contributes to the development of PSI global therapeutic strategy in line with PSIs indication-specific portfolio.
Assists in the development and maintenance of indication-specific KOL and specialist network.
Builds working relationships and maintains communication with all business stakeholders.

Qualifications

At least 10 years' experience in clinical research CRO/pharma environment.
MD or Pharmacy education background, specific in Oncology.
Knowledge/experience in expanding local clinical development activities from China to overseas (esp. Europe and/or US)
Client facing – must be comfortable travelling to other China cities for meetings/conferences
Ability to communicate with the rest of our global department – must possess business-level English standard

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.

About the Company

PSI CRO

Global CRO delivering on-time patient enrollment

PSI CRO is a global contract research organization that handles clinical trials for multiple therapeutic areas, with a focus on enrolling patients on schedule and delivering studies on time. Its services span feasibility assessments, trial planning, site selection, patient recruitment, and multi-continent trial execution across 50+ countries, backed by medical doctor resources dedicated to accurate timeline predictions. Unlike many CROs, PSI emphasizes predictable enrollment and on-time project delivery, aiming for high client satisfaction and repeat business through a pragmatic, no-nonsense approach. The company’s goal is to be regarded as the best CRO in the world by both clients and employees, achieved through reliable timelines, strong execution, and low staff turnover.

Company size: 1,001-5,000
Company stage: Not listed
Total funding: Not listed
Headquarters: Switzerland
Founded: 1995

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