Senior Clinical Project Manager

TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.

As part of our SRS/FSP team you will be dedicated to one sponsor a global pharmaceutical/biotech company.

Role Overview:

We are seeking a talented (Senior) Clinical Project Manager with a minimum of six years of experience in overseeing clinical trials and development projects within the pharmaceutical or biotechnology sectors. In this pivotal position you will be instrumental in driving the Clinical Development of lead compound currently in phase 1a and will play a crucial role in the planning of phase 1b and subsequent global studies. Reporting directly to the Chief Medical Officer you will collaborate closely with internal and external stakeholders to ensure alignment of objectives timelines risk management and budget throughout the development process.

Responsibilities:

Collaborate with Clinical CROs and internal teams to align trial objectives timelines risk assessment and budget while maintaining highquality standards.

Lead strategic and operational planning of the clinical development plan including regulatory strategy and interactions.

Engage with key opinion leaders and experts to support clinical development strategy and planning.

Develop and maintain comprehensive project plans encompassing timelines resource allocation risk assessment and budget for future trials.

Serve as the clinical development representative in the compound project team driving strategy and execution of the development plan.

Provide regular status updates to senior management and stakeholders facilitating informed decisionmaking.

Thrive in a global and virtual environment effectively operating across different time zones.

Qualifications:

Passion for clinical drug development and a commitment to making an impact on individuals affected by CNS disorders.

Minimum six years of experience in clinical development within the pharmaceutical or biotechnology industry.

Proven track record of successfully managing complex trials and projects through different drug development phases.

Regulatory Affairs experience in orphan disease product space preferably in CNS.

Strong leadership and interpersonal skills capable of motivating and guiding crossfunctional teams.

Independent selfmotivated and able to work efficiently.

Excellent communication presentation problemsolving and analytical abilities.

Bachelors or advanced degree in a relevant scientific or management field.

What We Offer:

We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll be joining a team that values collaboration innovation and making a difference in the lives of patients

A Bit More About Us:

Our journey began over 25 years ago in Sweden in the city of Lund. As a global CRO with the ultimate goal of ensuring patients safety and wellbeing we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe North America Asia Pacific and the Middle East.

Our core values of Trust Quality Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization.

#Together we make a difference