FAQs
What is the primary responsibility of the Sr Project Manager - FSP at Thermo Fisher Scientific?
The primary responsibility is to have global oversight for one or more studies of moderate complexity, managing all aspects of study execution from start-up through database close and inspection readiness, while ensuring timely delivery of quality study data.
What qualifications are required for this position?
Candidates should possess an MS/PhD with a minimum of 3 years of proven experience, or a BS/Nurse with a minimum of 5 years of proven experience, along with extensive global clinical trial/study management experience and knowledge of Good Clinical Practices.
Will this role require working with external partners?
Yes, this role involves providing quality oversight to Contract Research Organizations (CROs) and working closely with functional lines and CRO line functions to resolve site-level issues.
What skills are crucial for success in this role?
Crucial skills include strong problem-solving abilities, excellent communication skills in English, detail orientation, the ability to interpret study-level data, and understanding of protocol implementation feasibility.
Is leadership experience necessary for this position?
Yes, demonstrated study management and leadership experience is essential, including oversight of CROs and the ability to manage per subject costs and vendor projections.
What kind of work environment can a candidate expect in this role?
The candidate will be embedded within a client-dedicated team, working alongside experienced personnel from both the client and PPD colleagues to deliver innovative clinical support.
What attributes are emphasized in the company culture at Thermo Fisher Scientific?
The company emphasizes values such as Integrity, Intensity, Innovation, and Involvement, valuing diverse experiences, backgrounds, and perspectives among its employees.
How does Thermo Fisher Scientific ensure inspection readiness?
The Sr Project Manager is accountable for leading inspection readiness activities related to study management and site readiness throughout the clinical trial process.