Study Operations Manager

The Country Study Operations Manager (cSOM) is responsible for regional/country level activities from study startup through conduct and study close. The cSOM partners with the Global Study Manager, Study Start Up Project Manager, Site Intelligence Lead, Site Care Partners, Contracts Lead, Regulatory Affairs, pCRO and others as required to ensure a coordinated approach to study start up, execution and close out. The cSOM has comprehensive knowledge in managing and coordinating specific tasks and responsibilities as part of the larger Study Management team. The cSOM may help guide the Study Management strategy by inputting local intelligence and providing accurate updates on tasks delegated to them in order to support establishment of critical path activities and risks. The cSOM ensures the operational delivery of responsible tasks within the assigned studies, in accordance with the appropriate quality standards including ICH/GCP standards, SOPs, local operating guidelines and local regulatory requirements, as applicable.

Accountable for the execution of tasks and developing solutions to problems as needed to support deliverables. The cSOM will be accountable and responsible for tasks as designated on the study by the Global Study Manager which may include:

Regional/Country level implementation of Startup and Site Activation Plans

Regional/Country level Recruitment Strategy

Responsible for development of country level plans

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

Responsible for country vendor management and oversight including follow up and coordination of vendor deliverables

Responsible for ensuring the follow up and coordination of Regional/site QEs, PDs, data issues, metrics review, site issues/risks, audit responses, etc.

Work independently and exercise their own judgement.

Responsible for management/oversight of regional/country level activities from study startup through conduct and study close

May manage the study start up process in countries assigned and/or oversee pCRO responsible for these activities as applicable

Through the Site Care Partner, supports the Country/investigator outreach process, site identification and feasibility ensuring countries/sites can meet all study protocol requirements

Provides country level input on Startup and Recruitment milestones as provided by Site Care Partner to Global Study Manager during planning

Is accountable for overseeing Site Care Partner for assigned studies at country level in accordance with the overall project plan, manages and maintains accurate country level plans (e. g. timelines, budget, risk and quality plans)

Collaborates with accountable roles to identify and manage deviations and risks in study startup and execution and implements mitigation strategies as required. Is also accountable for resolution of Site Activation escalations to Study Teams including offering options for mitigation

Leader of the Local Study Team (core members: Site Care Partners, ad hoc members: ICL, Site Activation Partner, CTRO and Local Regulatory, Medical Affairs colleagues and other key stakeholders as required)

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.

Liaise with Site Care Partner, Site Activation Partners and Regulatory colleagues in

country to agree on submission strategy to Health Authorities and Ethic Committees

Utilizes roles in country such as Site Care Partner, and expert roles such as Contracts Leads, Site Activation Partners to provide the Global Teams with local intelligence and operational nuances to be considered

Follows up on region/country level issue status to ensure resolution.

Identifies country level trends to improve deliverables processes as needed

Utilizes country intelligence to provide input on country specific risks into preparation of Investigational Quality Management Plan, Study Monitoring Plans, ensures PTMF completeness and oversight of all relevant compliance activities for allocated studies

Ensures audit/Inspection readiness during start-up and conduct

Manages applicable Quality Events with local team as applicable and required

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

Responsible to drive and ensure delivery of data cleaning deliverables for pCRO and sites as applicable

Provides input on Country level Per Subject Costs, local vendor costs and other fees where applicable

May act as a Subject Matter Expert

May lead operational effectiveness initiatives at country or regional level

Responsible for PTA and SIV report review for reports completed by the Site Care Partner

Supports implementation of Pfizer's Site Technology Experience systems (e. g. Shared Investigator Platform SIP, Centralized Account Management CAM)

Support to EC/RA and other relevant (e. g. radiation, biobank) submissions and deficiency/query responses for initial and subsequent CTA submissions within required timelines

Drives pCRO and/or applicable internal study team members to ensure PTMF set up meets study requirements, and maintains oversight of PTMF completeness

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

Ensures applicable internal study team members maintain appropriate level IP/equipment/ancillary supplies management including Import/Export License management with the support of Clinical Trial Assistants and other roles as required

Supports implementation of new tools and technologies (e. g. eConsent, eISF, Remote Source Access, remote SDV/SDR, iConnect, implementation of protocol required decentralized trial options etc. )

Support Identification, contract development and management of local vendors or facilities as per protocol

Investigator Meeting support and management including doing presentations as appropriate

Management of local Investigator Meetings including doing presentations as appropriate

BASIC QUALIFICATIONS

• Relevant operational Clinical Trial experience. A scientific or technical degree is preferred along with knowledge of clinical trial methodology

• MBA/MS 3+ years of relevant experience

• BA/BS 5+ years of relevant experience

• BS/BSc/MS/MSc

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

• English is required.

Prior Experience

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 and working in a matrix management environment

Skills and Technical Competencies

Expertise in the use of study/site dashboard and reporting tools

Detail oriented & possesses technical expertise

Ability to manage moderately complex processes

Ability to operate in a matrix environment

Risk Identification & Mitigation

Strategic Planning, Analytical and Problem-Solving Skills

Critical Path Analysis

Excellent communication skills, both written and verbal

Ability to adapt to changing technologies and processes

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

Medical

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