Clinical Project Manager (up to Lead or Senior level) at PSI CRO

Tokyo, , Japan -

Full Time

Start Date

Immediate

Expiry Date

13 Sep, 26

Salary

0.0

Posted On

15 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Project Management, Global Clinical Research, Budget Management, Team Leadership, Stakeholder Management, Bid Defense, Proposal Development, Compliance, Oncology, Rare Disease, Phase II Clinical Trials, Phase III Clinical Trials, English Proficiency, Japanese Proficiency, Resource Allocation, Negotiation

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is an award-winning full-service CRO, bringing together more than 2,700 dynamic and knowledgeable individuals working to help impact the future of medicine in more than 60 countries around the world. We support pharmaceutical, biotechnology, and medical device companies with the services needed to perform clinical trials of new medicines. Our work helps patients in need improve their well-being – a fundamental driver for many of us to show up and do our best each day. Job Description Take your career to the next level and lead challenging full-service global clinical research projects, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study. Your responsibilities will include: (Tokyo or Osaka office) Management of country/regional aspect of global, multi-center clinical research projects in a variety of therapeutic areas Delivery of clinical research projects on time, within budget and in accordance with high quality standards Leading and managing multi-functional project teams Training, mentoring and coaching project team members Being the primary point of contact to client on all project matters Attending bid defense meetings, participating in development of proposals and client presentations Implementation of company standard practices and compliance with intradepartmental procedures Qualifications Recent clinical research experience in the capacity of project manager or equivalent (e.g. Clinical Trial Manager, Clinical Study Team Lead, etc.) Global or regional clinical project management experience, including management of all project services from startup to closure Therapeutic experience in oncology, and/or MS, IBD, hemophilia, other rare disease, infectious diseases is preferred Experience managing Phase II and III clinical projects is preferred BSc or MSc in Life Sciences (or similar) or an equivalent combination of education, training & experience Excellent communication skills, both written and verbal, with the ability to build strong internal and external stakeholder relationships Ability to negotiate confidently Team building, resource allocation and organizational skills are essential Full working proficiency in English and Japanese to work with global teams and clients Additional Information Make the right call and take your career to a whole new level, where quality is the cornerstone of your work and training. If shortlisted for an interview, our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your interview experience smooth and comfortable.

Responsibilities

Lead and manage full-service global clinical research projects, ensuring delivery on time, within budget, and according to quality standards. Act as the primary point of contact for clients and manage multi-functional project teams across various therapeutic areas.