Clinical Trial Manager I

Based on Regional or Country Practices official titles will vary for this level) Performs the role of Clinical Trial Manager (CTM) including operational oversight of assigned protocol(s) from start-up through to database lock and closeout activities as described in GCO procedural documents.

. CTM is a person within Trial Co-ordination and Site Management responsible for local management of a trial (or Medical Affairs data generation activities) in a country or countries. The CTM is the primary point of contact at a country level for assigned studies.

The CTM is responsible for coordinating and leading the local trial team in order to deliver quality data and trial documents/records that are compliant with assigned protocol, codes of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs) and regulatory requirements. CTM actively contributes to process improvement; training and mentoring of Clinical Trial Assistants Site Managers and CTMs. The CTM may have some site management responsibilities.  An CTM I usually performs principal responsibilities under the direct supervision of an CTM II or III and/or Functional Manager

Principle Responsibilities:

1. Is responsible for country do-ability (if applicable) and site feasibility assessment in conjunction with CTA (if applicable), SM and GTM. Implements any local criteria for site selection. Ensure consistent conduct of pre-trial assessment visits and instruct teams on appropriate follow-up of pre-trial visit report and country feasibility report. Recommends suitable sites for selection to participate in trial.
2. Collaborates with the CPL, GTM, local management/Country Head and Protocol Owner to select final site list.
3. Contributes input to the Trial Plan, Safety Monitoring Plan, Filing and Archiving Plan and Investigational Product documents at a country level or initiates development of these plans for a single country trial.
4. Leads and coordinates local trial team activities in compliance with GCO Standard Operating Procedures (SOP), Work Instructions (WI) and applicable regulations. Leads local project planning activities to meet recruitment targets and to deliver high quality data on time and within study budget. Including but not limited to: development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting.
5. Ensures that all SAEs/PQCs are reported within reporting timelines and documented as appropriate.
6. Maintains and updates trial management systems (e.g. CTMS, eTMF/LAF, Trial Master Source and Sharepoints). Uses study tools and management reports available to analyze trial progress.
7. Monitors country progress and initiates corrective and preventive actions when the trial deviates from plans and communicates study progress and issues to study management teams.
8. May submit requests for vendor services and may support vendor selection
9. May lead negotiation of trial site contracts and budgets, with the assistant from a CTM II or III. Forecasts and manages country/local trial budget to ensure accurate finance reporting and trial delivered –within budget. Adheres to finance reporting deliverables and timelines.
10. Attends/participates in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting.
11. Conducts local trial team meetings and provides or facilitates SM training when needed (i.e. implementation of study amendment-and changes in study related processes).
12. Reviews and approves Monitoring Visit Reports submitted by SM; identifies issues and/or trends across a trial project and escalates deviation issues to the GTM and FM as needed
13. Reviews and approves site and local vendor invoices as required
14. Works with SM to ensure CAPP is implemented for audits and inspection or any quality related visits
15. Complies with relevant training requirements.
16. Acts as local expert for assigned protocols. Develops strong therapeutic knowledge to support roles and responsibilities. May represent Global Clinical Operations on cross functional teams.
17. Acts as primary local/country contact for a trial. Establishes and maintains excellent working relationships with external stakeholders, in particular investigators, study trial coordinators and other site staff; and internal stakeholders, including Medical Affairs and Marketing for Medical Affairs trials.
18. Actively contributes to process improvement.

Principle Relationships:

• Reports to Functional Manager
• Internal Interfaces: Functional Manager, Partner with the CTAs, SMs, Quality & Compliance Managers/Experts, Contracts and Grants associates, GTM, R&D study team (e.g., SRP), protocol owners, data management and Medical Affairs (when applicable) to ensure overall trial coordination and site management activities for assigned protocols.

External Interfaces:  Trial Site Personnel, external vendor representatives

Education and Experience Requirements/Qualifications:

• A minimum of a BA/BS degree is required. A degree in a health or science related field is preferred.
• Specific therapeutic area experience may be required depending on the position. Should have basic understanding of the drug development process including ICH/GCP and local regulatory requirements.
• Solid communication and computer skills required.
• Proficient in speaking and writing the country language and English language. Good written and oral communication skills

At ICON, inclusion & belonging are fundamental to our culture and values.   We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status