Country Study Operations Manager - FSP

Parexel FSP is looking for multiple Country Study Operations Manager I roles ! Candidates can be based anywhere in Mexico and Argentina.

Job Summary

The Country Study Operations Manager I (cSOM I) has responsibilities for study and specific country level activities from study startup through conduct and study close on studies of limited complexity (a small number of countries/sites) or manages portions of a larger study (such as recruitment and retention).

Key Accountabilities : 

Study Management Oversight  

 Supports Global Study Managers (GSMs), other SOMs, and the larger study management delivery of the study by leading specific parts of the project, driving specific countries, executing tasks of moderate complexity, and developing solutions to problems as needed to support deliverables 

Serves as leader of the local study team (core members, ad hoc members, and other key stakeholders as required) on one or more studies 

 Oversees the preferred Contract Research Organization (pCRO) and/or Country Trial Manager (CTM)/Site Care Partner (SCP) for assigned studies at country level in accordance with the overall project plan, and manages and maintains accurate country level plans (e.g., timelines, budget, risk, and quality plans) 

May manage the study start up process in countries assigned [where the Start Up Project Manager (SUPM) is not assigned] and/or oversee the pCRO responsible for these activities as applicable 

Liaises with SCP, Lead SCP, Site Activation Partners (SAPs), and regulatory colleagues in country to agree on submission strategy to Health Authorities (HAs) and Ethic Committees (ECs) 

Provides country level input on startup and recruitment milestones as provided by pCRO and/or CTM/SCP to GSM during planning 

Collaborates with accountable roles to identify and manage deviations and risks in study startup and execution and implements mitigation strategies as required. Accountable for resolution of site activation escalations to study teams including offering options for mitigation 

May be responsible and accountable for, as designated by the GSM: 

o Regional, country and study level implementation of startup and site activation plans (through SUPM or pCRO if assigned) 

o Regional, country and study level recruitment strategy 

o Support of the development of study level plans 

o Communication with the local team and internal stakeholders and pCRO as applicable to ensure efficient and timely study delivery of the agreed plans 

o Study and/or country vendor management and oversight including follow up and coordination of vendor deliverables 

o Assurance of the follow up and coordination of regional and site quality events, protocol deviations, data issues, metrics review, site issues and risks, audit responses, etc.  

Study Management Operations  

May help guide the study management strategy by contributing local intelligence and providing accurate updates on delegated tasks to support establishment of critical path activities and risks 

May independently take on activities with instruction provided as needed 

Through the SCP, CTM or pCRO, supports the country and investigator outreach process, site identification and feasibility ensuring countries and sites can meet all study protocol requirements 

Ensures compliance to relevant global and local, internal and external requirements, and regulations 

Ensures timely communication bidirectionally between the global and local study team. Provides protocol level guidance and support to responsible local study team members as applicable 

Follows up on region and country level issue status to ensure resolution 

Identifies country level trends to improve deliverables processes as needed 

Ensures audit and inspection readiness during start up and conduct 

Manages applicable quality events with pCRO and local team as required 

Drives and ensures delivery of data cleaning deliverables for pCRO and sites as applicable 

Reviews Pre-Trial Assessment and Site Initiation Visit reports completed by SCPs 

Coordinates effective site recruitment planning to allow for implementation of plans at the country and site level, consistent with global plan and local targets 

Drives pCRO and/or applicable internal study team members to ensure Trial Master File (TMF) set up meets study requirements, and maintains oversight of TMF completeness 

Ensures pCRO and/or applicable internal study team members maintain appropriate level Investigational Product (IP), equipment and ancillary supplies management including import/export license management with the support of Clinical Trial Assistants (CTAs) and other roles as required 

Supports identification, contract development and management of local vendors or facilities as per protocol 

May lead and guide the closing out of one or more studies of low complexity post database lock 

Provides Investigator Meeting (IM) support and management, including conducting presentations as appropriate 

Provides country level documents to TMF and maintains oversight of Investigator Site File (ISF) reconciliation and completeness actions 

Provides support to ECs, Regulatory Authorities (RAs), and other relevant (e.g., radiation, biobank) submissions and deficiency and query responses for initial and subsequent Clinical Trial Application submissions within required timelines 

Ensures the operational delivery of responsible tasks in accordance with the appropriate quality standards including ICH GCP standards, SOPs, local operating guidelines, and local regulatory requirements, as applicable 

Subject Matter Expertise  

Acts as the point of contact for all study level questions for the local study team, ensuring resolution at lowest possible level, and when needed liaising with and escalating to appropriate global roles and teams 

May lead operational effectiveness initiatives at country or regional level 

Utilizes roles in country such as Lead SCP, and expert roles such as Contracts Leads and SAPs, to provide the global teams with local intelligence and operational nuances to be considered 

Provides input on country level per subject costs, local vendor costs, and other fees where applicable 

Utilizes country intelligence to provide input on country specific risks into preparation of Investigational Quality Management Plan and Study Monitoring Plan, and ensures Trial Master File (TMF) completeness and oversight of all relevant compliance activities for allocated studies 

Supports implementation of client’s site technology experience systems 

Supports implementation of new tools and technologies (e.g., eConsent, eISF, remote source access, remote source data verification/review (SDV/SDR), iConnect, implementation of protocol required decentralized trial options) 

Compliance with Parexel standards  

Complies with required training curriculum 

Completes timesheets accurately as required 

Submits expense reports as required 

Updates CV as required 

Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements 

Skills:   

Expertise in the use of study and site dashboards and reporting tools 

Detail oriented and possesses technical expertise 

Ability to manage moderately complex processes 

Risk identification and mitigation, strategic planning, and critical path analysis skills 

Analytical and problem solving skills 

Ability to adapt to changing technologies and processes, work independently and exercise own judgement 

Supportive of an environment where innovation is standard, including developing ideas and taking appropriate risks to advance innovative processes 

Effective verbal and written communication skills in relating to colleagues and associates, both inside and outside of the organization  

Ability to operate in a matrix environment 

Fluency in written and spoken English required 

Ability to work outside of core business hours, as required, to support global trials or initiatives 

Ability to travel, as required, including Investigator Meetings, vendor kick off and re-set meetings, and client internal global or department level meetings 

Knowledge and Experience (preferred):  

Comprehensive knowledge of own discipline with good knowledge of other disciplines to ensure that the study can meet its goals and to serve as a resource for others 

Comprehensive knowledge in managing and coordinating specific tasks and responsibilities as part of a larger study management team 

Working knowledge of Good Clinical Practice, clinical and regulatory operations, and environment in countries under responsibility 

Demonstrated clinical research experience and/or study management/startup project manager experience 

Demonstrated experience in managing country level operational activities and/or vendors 

Experience in study and quality management 

Knowledge of clinical trial methodology 

Experience working in a matrix management environment 

Relevant operational clinical trial experience  

o See below Education section for minimum requirements 

Education:  

Bachelor’s of Science or Bachelor’s of Arts degree with a minimum 5 years of relevant operational clinical trial experience required 

Master’s of Science or Master’s of Business Administration degree with a minimum 3 years of relevant operational clinical trial experience required 

A scientific or technical degree is preferred 

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