Clinical Trial Coordinator II - FSP

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Trial Coordinator II – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to provide administrative and technical support to the Project Team. As a Clinical Operations Delivery Associate II, you'll support audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document. You will provide administrative support for site activation activities and aid in the development of the critical path for site activation within assigned projects to support rapid site activations. Representing the organization in the global medical research community, you may develop collaborative relationships with investigators and site personnel to conduct feasibility assessments in accordance with feasibility processes and within deliverable timelines. You may develop a local knowledge base of sites in the respective market through collaboratively working with local company personnel. Additionally, you may utilize local knowledge, organization systems, external site lists, and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. You may act as a buddy during the onboarding phase, support training of new staff, and participate in departmental initiatives to aid in process improvements and enhancements.

What You’ll Do:

• According to the specific role (Central or Local), 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, including, but not limited to, study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients and tracking of project level activity plans in appropriate system. 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

• May support scheduling and organization of client and/or internal meetings with completion of related meeting minutes.

• 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.

• May support start-up team in Regulatory submissions.

• 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. Ensure current investigator and site staff contact details are appropriately maintained in company systems.

• May complete the ‘Site Interest Plan’ in CTMS and collection and delivery of associated documents from investigators and site personnel. Document in real time all communication, attempts and follow up associated with site contact and survey responses.

• 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. Ensure compliance with the plan and escalates concerns/non-compliance to management.

• May act as the local expert regarding site capacity and experience. Work with key local personnel to gather knowledge base and recommend additional sites. Harnesses this knowledge base when performing local tiering of sites.

• 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.

Education and Experience Requirements:

• Bachelor's degree preferred.

• •Previous experience in a CTC role that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years as a CTC).

• Must have experience in Veeva eTMF, CTMS

• Should have worked in Global Clinical Trial and coordinated with Local/Global Team members

• Having experience in Vendor Management is preffered

Knowledge, Skills and Abilities:

• 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 local 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

• Ability to manage risk and perform risk escalation appropriately

Working Conditions and Environment:

• Work is performed in an office/ laboratory/clinical/ and/or home office environment with exposure to electrical office equipment.

• Occasional drives to site locations. Potential Occasional travel required.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.