Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Feasibility Site Specialist

Summary

This is an outstanding opportunity to join Thermo Fisher Scientific Inc. in a pivotal Research role located in Taiwan. As a Trial Activation Feasibility Specialist II, you will lead the charge in ensuring the flawless execution of feasibility assessments. You will be instrumental in developing collaborative relationships with investigators and site personnel, driving our strategic site development goals while adhering strictly to timelines.

Essential Functions and Other Job Information:Collaborate closely with the local clinical operations management head and Feasibility Manager (FM).Initiate feasibility intelligence collection based on study needs.Vet local site lists, applying internal and external sources to ensure alignment with the defined site profile.Identify risks to quality and compliance proactively, and implement mitigation plans.Maintain current investigator and site staff contact details within Thermo Fisher Scientific systems.Document all communication attempts and follow-ups associated with site contact and feasibility documents in real-time.Manage primary investigator changes for sites in the relevant system.Review the DPA/ISD status of each site, tracking documents as needed.Support the review and logical assessment of survey data, updating relevant systems with appropriate questionnaire statuses.Achieve targeted response goals for assigned projects and communicate site issues and feasibility risks.Ensure an efficient plan for site contact and follow-up, raising concerns to the Feasibility Manager as needed.Serve as the local guide on site capacity and expertise, recommending additional sites where applicable.Champion the inclusion of strategic sites into the feasibility process.Conduct phone interviews with physicians and site personnel to gather protocol-level input and support trial optimization projects.Conduct on-site visits when applicable.Provide local knowledge for the identification and development of new sites.Expand therapeutic knowledge to assist in reviewing local country site lists.Collect data on site capabilities, including electronic medical records and remote source document verification, coordinating with relevant departments.

Education and Experience:Associate's degree or equivalent relevant formal academic/vocational qualification.Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’).

Knowledge, Skills, and Abilities:Effective oral and written communication skills for engaging with medical personnel and internal teams.Strong attention to detail, quality documentation, and negotiation skills.Proficiency in the local language and good command of English.Ability to work in a team or independently, as required.Working knowledge of GCP and applicable SOPs.Ability to thrive in a matrix environment and build positive relationships.Interest in managing risk and effectively resolving critical issues.

Benefits

We offer competitive remuneration, an annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific provides employment with an innovative, forward-thinking organization and outstanding career and development prospects. Join us for an exciting company culture that stands for integrity, intensity, involvement, and innovation!