Clinical Trial Coordinator

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🕒 May 26

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix • Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system(s) • Ensures allocated tasks are performed on time, within budget and to a high quality standard • Proactively communicates any risks to project leads and line manager as appropriate • Performs administrative tasks on assigned trials including but not limited to timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, distributing mass mailings and communications as needed, providing documents and reports to internal team members • Reviews and tracks local regulatory documents • Analyzes and reconciles study metrics and findings reports • Assists with clarification and resolution of findings related to site documentation • Maintains vendor trackers • Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites • Assists with study-specific translation materials and translation QC upon request • Assists with technical and administrative support for projects in collaboration with internal departments and team members • Maintains knowledge of and understands SOPs, client SOPs/directives, and current regulatory guidelines as applicable to services provided • Ensures that trial status information relating to activities is accurately maintained in the database and current at all times • Where applicable, develops and maintains relationship with client local affiliates • Champions the inclusion of Strategic Collaboration sites into the process • Where applicable, conducts on-site feasibility visits (Asia Pac only) • Trains new personnel in processes and systems • May support the maintenance of study specific documentation and global support with specific systems, tools and trackers • Ensures (e)TMF is up to date by following file review schedules and documenting findings in appropriate system(s) • May provide system support (i.e., Activate & eTMF) • May support RBM activities • May transmit documents to client and centralized IRB/IEC • May attend Kick off Meeting and take notes when required • May support scheduling of client and/or internal meetings • Provides support as needed to coordinate with internal departments and ensure site start-up activities within the site activation critical path are aligned • Assists the project team with the preparation of regulatory compliance review packages • Occasionally works directly with site(s) to obtain documents related to site selection • May develop site list, including research from internal and external sources to ensure the site list is reflective of the defined site profile • Supports the review of survey data to ensure responses are logical, complete and reflective of the question asked • Works in collaboration with teammates to achieve targeted deadlines for assigned projects • Communicate with the team and appropriate clinical personnel regarding site issues and risks • Ensures an efficient, effective plan is in place for site contact and follow up • May act as the local expert regarding site capacity and experience • May conduct phone interviews, scripted or non-scripted, with physicians and other site personnel to discuss standard of care and obtain protocol-level input to support trial optimization projects • Liaises with Global Investigator Services to resolve investigator queries in real time and maintain ‘accounts and contact’ information • Contributes to the development and roll-out of global strategic feasibility processes and best practices

🎯 Requirements

• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification • Bachelor's degree preferred • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years) • Ability to work in a team or independently, as required • Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively • Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency • Strong customer focus • Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines • Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non clinical/clinical aspects of project implementation, execution and closeout • Excellent English language and grammar skills and proficient local language skills as needed • Good presentation skills • Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems • Ability to successfully complete the organizations clinical training program • Self-motivated, positive attitude with effective strong interpersonal skills • Effective oral and written communication skills, with the ability to communicate effectively with medical personnel • Excellent interpersonal skills • Strong attention to detail and quality of documentation • Good negotiation skills • Good computer skills and the ability to learn appropriate software • Fluency in Latvian language as well as a good command of the English language and grammar skills • Basic medical/therapeutic area and medical terminology knowledge • Ability to work in a team environment or independently, under direction, as required • Basic organizational and planning skills • Basic knowledge of local health systems • Ability to attain and maintain a working knowledge of GCP and applicable SOPs • Excellent customer focus • Proven flexibility and adaptability • Ability to work in a matrix environment • A proven relationship builder • An independent thinker

🏖️ Benefits

• Flexible working arrangements • Professional development opportunities • Health insurance • Paid time off