Country Study Operations Manager I

Job title:

Country Study Operations Manager I

Company:

Pfizer

Job description

Country Study Operations Manager I – Italy will report into Lorenzo Majerini Director/Supervisor of Study ManagementJOB SUMMARYThe Study Operations Manager will have responsibilities for study and regional or specific country level activities from study startup through conduct and study close. The Study Operations Manager has responsibility for study management aspects of assigned studies of limited complexity (e.g. single country, a small number of countries/sites) or manage a unique part of a larger study (e.g. recruitment and retention). The Study Operations Manager will be assigned to one or more studies and will be tasked with taking on responsibilities in support of Global Study Managers, other Study Operational Managers and the larger Study Management delivery of the study. The Study Operations Manager may partner with the Global Study Manager, Study Start Up Project Manager, Site Intelligence Lead, Country Trial Manager, Site Care Partners, Site Excellence Partners, Site Relationship Partners, Contracts Lead, Regulatory Affairs, pCRO and others as required to ensure a coordinated approach to study start up, execution and
close out.
The Study Operations Manager has comprehensive knowledge in managing and coordinating specific tasks and responsibilities as part of the larger Study Management team. The Study Operations Manager I may lead specific
parts of the project or drive specific countries. They 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. They will ensure the operational delivery of responsible tasks within one or more studies, in accordance with the appropriate quality standards including ICH/GCP standards, SOPs, local operating
guidelines and local regulatory requirements, as applicable. The Study Operations Manager may be responsible to independently take on activities with instruction provided as needed. They may lead and guide the closing out of one or more studies of low complexity post database lock.
Accountable for the execution of tasks of moderate complexity and developing solutions to problems as needed to support deliverables. The Study Operations Manager will be accountable and responsible for tasks as designated on
the study by the Global Study Manager which may include:Regional/Country/Study level implementation of Startup and Site Activation Plans (through SUPM or pCRO if assigned)Regional/Country/Study level Recruitment StrategyResponsible to support the development of study level plansCommunication 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 plansResponsible for study and/or country vendor management and oversight including follow up and coordination of vendor deliverablesResponsible for ensuring the follow up and coordination of Regional/site QEs, PDs, data issues, metrics review, site issues/risks, audit responses, etc.The Study Operational Manager will be able to work independently and exercise their own judgement.JOB RESPONSIBILITIESOperational Study ManagementResponsible for management/oversight of study and regional/country level activities from study startup through conduct and study closeMay manage the study start up process in countries assigned (where SUPM not assigned) and/or oversee pCRO responsible for these activities as applicableThrough the Site Care Partner/Country Trial Manager or pCRO supports the Country/investigator outreach process, site identification and feasibility ensuring countries/sites can meet all study protocol requirementsProvides country level input on Startup and Recruitment milestones as provided by pCRO and/or Country Trial Manager/Site Care Partner to Global Study Manager during planningIs accountable for overseeing pCRO and/or Country Trial Manager/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 mitigationLeader of the Local Study Team (core members: (Lead) Site Care Partners Clinical Trial Assistant, 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 regulationsEnsures 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, Lead Site Care Partner, Site Activation Partners and Regulatory colleagues in country to agree on submission strategy to Health Authorities and Ethic CommitteesUtilizes roles in country such as Lead 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 consideredActs as the study level 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/teamsFollows up on region/country level issue status to ensure resolution.Identifies country level trends to improve deliverables processes as neededUtilizes 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 studiesEnsures audit/Inspection readiness during start-up and conductManages applicable Quality Events with pCRO and local team as applicable and requiredCoordinates effective site recruitment planning to allow for implementation of plans at the country and site level, consistent with global plan and local targetsResponsible to drive and ensure delivery of data cleaning deliverables for pCRO and sites as applicableProvides input on Country level Per Subject Costs, local vendor costs and other fees where applicableMay act as a Subject Matter ExpertMay lead operational effectiveness initiatives at country or regional levelResponsible for PTA and SIV report review for reports completed by the Site Care PartnerSupports 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 timelinesDrives pCRO and/or applicable internal study team members to ensure PTMF set up meets study requirements, and maintains oversight of PTMF completenessProvides country level documents to PTMF and maintains oversight of Investigator Site File (ISF) reconciliation and completeness actionsEnsures pCRO and/or 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 requiredSupports 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 protocolInvestigator Meeting support and management including doing presentations as appropriateManagement of local Investigator Meetings including doing presentations as appropriateBASIC QUALIFICATIONS:Training and EducationRelevant operational clinical trial experienceA scientific or technical degree is preferred along with knowledge of clinical trial methodologyBA/BS 5+ years of relevant experienceMBA/MS 3+ years of relevant experienceBS/BSc/MS/MScWorking knowledge of Good Clinical Practice, clinical and regulatory operations and environment in countries under responsibilityEnglish is required.Prior ExperienceDemonstrated clinical research experience and/or study management/startup project manager experienceDemonstrated experience in managing country level operational activities and/or vendorsExperience in Study and Quality management and working in a matrix management environmentSkills and Technical CompetenciesExpertise in the use of study/site dashboard and reporting toolsDetail oriented & possesses technical expertiseAbility to manage moderately complex processesAbility to operate in a matrix environmentRisk Identification & MitigationStrategic Planning, Analytical and Problem-Solving SkillsCritical Path AnalysisExcellent communication skills, both written and verbalAbility to adapt to changing technologies and processesPurposeBreakthroughs that change patients’ lives… At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.Digital Transformation StrategyOne bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.FlexibilityWe aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!Equal Employment OpportunityWe believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!Medical#LI-PFE

Expected salary

Location

Roma

Job date

Thu, 17 Oct 2024 07:18:47 GMT

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