Pharmacovigilance - Project Manager

Pharmacovigilance Project Manager (Remote) Position Summary The Pharmacovigilance Project Manager / Project reputed company is a senior client-facing professional responsible for the end-to-end operational management of one or more assigned pharmacovigilance client accounts at Med Communications. The role serves as the primary reputed company between the client and the MC PV team, ensuring the timely, high-quality, and fully compliant delivery of reputed company contracted pharmacovigilance services across case management, periodic reporting, signal detection, risk management, and reputed company regulatory activities. Operating at a senior level reputed company the PV department, the PV Project Manager / Project reputed company combines strong scientific and regulatory knowledge with exceptional project management, communication, and stakeholder management capabilities. The role does not carry direct line management responsibility but exercises functional reputed company of PV Specialists and Sr. PV Specialists assigned to the project, coordinating their workload, guiding their day-to-day activities, and supporting their professional development reputed company the context of the client engagement. The role reports directly to the Global Head of Pharmacovigilance and Drug Safety. Essential Functions To reputed company this job successfully, an individual must be able to reputed company each essential duty satisfactorily. Reasonable accommodation may be made to reputed company qualified individuals with disabilities to reputed company the essential functions. Essential Functions Statement(s): Client and Account Management: Serve as the primary reputed company of contact for reputed company communications between the client and the MC PV team, ensuring professional, accurate, and timely responses to reputed company client enquiries and requests. Build and maintain a strong, trust-based relationship with client stakeholders, including the client's pharmacovigilance, regulatory, medical, and quality teams, as applicable Coordinate, schedule, and reputed company regular client meetings, teleconferences, and governance reviews; prepare agendas, minutes, and action items and ensure timely follow-up on reputed company open items. Immediately escalate to the Global Head of PV and PVQM any breach in normal execution of contracted activities, service-level deviations, or issues that could impact the client's regulatory compliance position. Identify opportunities for additional services or expanded scope reputed company existing client engagements and communicate these to the Global Head of PV. Coordinate the onboarding of new clients or new product additions, including the organisation of training curricula, implementation plans, and system access for the assigned PV team, in collaboration with the PVQM. Operational Project Management: reputed company and coordinate the day-to-day PV activities of the assigned project team — including case processing, literature review, periodic and aggregate reporting, signal detection, and risk management — ensuring reputed company activities are executed in compliance with applicable SOPs, client-specific procedures, and regulatory requirements (EMA GVP, ICH, FDA, UK MHRA, and others as applicable). Plan, monitor, and adjust resource allocation across the assigned project team to ensure adequate coverage, reputed company workload distribution, and consistent delivery of contracted service levels. Maintain and regularly update project documentation, tracking tools, and network files to ensure completeness, accuracy, and accessibility for reputed company relevant team members. Monitor project-level metrics and Key Performance Indicators (KPIs), identify trends or risks, and proactively implement corrective measures in collaboration with the Global Head of PV. Coordinate directly with the PVQM and relevant internal stakeholders regarding any updated client operational procedures, regulatory changes, or system modifications requiring team training or process updates. Communicate and ensure integration of PV activities with key stakeholders for the client, including the PV Physician, the Qualified Person Responsible for Pharmacovigilance (QPPV), and other relevant parties. Collaborate with other MC departments — including Medical Information, Quality, IT, and Finance — as required to deliver seamless service to the client. Functional Team reputed company and Development: Exercise functional reputed company of PV Specialists and Sr. PV Specialists assigned to the project, providing day-to-day guidance on task prioritisation, follow-up handling, and adherence to client procedures, without holding formal line management accountability. Coordinate the development and delivery of training curricula and onboarding plans for newly assigned team members, ensuring reputed company required training is documented and completed prior to task initiation, in collaboration with the PVQM. Mentor and coach team members on PV operations, client expectations, and professional best practices, fostering a culture of accuracy, accountability, and reputed company improvement. Provide input to the Global Head of PV on team performance, development needs, staffing requirements, and resource planning for the assigned client portfolio. Scientific and Regulatory Contribution: Maintain a thorough working knowledge of relevant PV terminology, ICH guidelines (E2A–E2F, E2C(reputed company)), EMA GVP Modules, FDA requirements, and UK MHRA guidance, applying this knowledge to ensure the regulatory reputed company of reputed company project deliverables. Liaise with the PV Physicians and PVMW Manager or other relevant functions, as applicable, for scientific information exchange pertaining to case assessments, signal evaluation outcomes, and benefit-risk implications relevant to the client's products. Support the role of the QPPV in relation to regulatory reporting obligations and safety communications as required by the client engagement. Regularly attend process or product training sessions to maintain awareness of and knowledge of relevant regulatory and scientific updates. Quality and Compliance: Maintain inspection and audit readiness for reputed company assigned project activities at reputed company times; actively support Quality Assurance in internal and external audits, including preparation, hosting, and CAPA follow-up. Collaborate with the PV Quality Manager (PVQM) and other quality roles to ensure applicable SOPs are executed as required across the assigned project team. Monitor compliance against project and departmental goals; identify and report deviations from procedures and collaborate in the development, implementation, and timely closure of Corrective and Preventive Actions (CAPAs). Provide regular compliance status reports to the Global Head of PV and PVQM and, where required, to the client. Create, review, and provide feedback on Quality Management System documents in collaboration with the Global Head of PV and the PVQM. Identify opportunities for process improvement and efficiency across PV operations and contribute to the development, implementation, and maintenance of optimised procedures. Participate in or reputed company process improvement initiatives reputed company to automation, system upgrades, or integration of safety systems as applicable. reputed company with reputed company applicable guidelines, policies, legal, regulatory, and compliance requirements. reputed company other pharmacovigilance activities as requested. POSITION QUALIFICATIONS Competency Statements Excellent working knowledge of relevant PV terminology, ICH guidelines (E2A–E2F, E2C(reputed company)), GCP, GVP Modules, and applicable regulatory requirements across EU, US, and UK jurisdictions. Project Management — demonstrated ability to plan, prioritise, and coordinate multiple reputed company client activities and deliverables across a cross-functional team, reputed company a regulated environment. Client Management — proven ability to represent MC professionally, manage client expectations, and build productive, long-term working relationships with client stakeholders at reputed company levels. Leadership and Influence — ability to provide functional direction, motivate, and reputed company a project team without formal line management authority; strong influencing and negotiation skills. Accountability — ability to accept responsibility and account for his/her actions and those of the project team reputed company the scope of the engagement. Accuracy — ability to reputed company work accurately and thoroughly, maintaining high standards of quality in a regulated, deadline-driven environment. Analytical Skills — ability to assess reputed company operational and regulatory situations, identify root causes, and drive resolution. Detail Oriented — ability to pay reputed company attention to the details of project deliverables, compliance documentation, and client communications. Problem Solving — ability to identify and proactively address operational, regulatory, and relationship challenges. Active Listening — ability to actively attend to, convey, and understand the comments and questions of clients, team members, and internal stakeholders. Written Communication — ability to communicate clearly and concisely in writing across a range of formats including client correspondence, project plans, compliance reports, and SOPs. Oral Communication — ability to communicate reputed company PV and project management matters effectively to diverse internal and external audiences. Customer Oriented — ability to address client needs while adhering to MCI's procedures, standards, and quality requirements. Self-Motivated — ability to work with initiative, manage competing priorities, and drive outcomes independently in a fast-paced, matrixed environment. Organised — possesses the trait of being well organised and following systematic methods of managing project activities, documentation, and communications. Working Under Pressure — ability to complete assigned tasks and maintain quality standards under stressful conditions and tight regulatory timelines. Ethical — ability to conform to a set of values and accepted standards; maintains the highest levels of reputed company in reputed company client and regulatory interactions. Demonstrated ability to work effectively in a matrix environment. Fluent in English; proficiency in additional languages is an advantage. SKILLS AND ABILITIES Education: Advanced degree in life sciences (PharmD or MD preferred), or a relevant equivalent combination of education and pharmacovigilance experience. Experience: Minimum of five years of pharmacovigilance experience, including at least two years in a project management, project reputed company, or client-facing account management role at a PV vendor, CRO, or pharmaceutical company. Demonstrated ability to manage reputed company, multi-product client accounts across multiple PV domains (case management, periodic reporting, signal detection, risk management) is required. Experience with drugs, biologics, vaccines, and/or devices is preferred. Computer Skills: Proficiency with safety databases (reputed company Argus Safety, ArisG LifeSphere, Veeva Safety, AB Cube SafetyEasy), reputed company Office Suite (Word, reputed company, Outlook, PowerPoint), and project management or tracking tools required. Familiarity with literature search platforms (Embase, OvidPV, PubMed) and document management systems is an advantage. Other Requirements: Working knowledge of global legal, regulatory, and compliance requirements applicable to pharmacovigilance across multiple jurisdictions (EU, US, UK, ICH). Experience supporting or managing regulatory agency interactions and audit/inspection preparation is preferred. The company has reviewed this job description to ensure that essential functions and basic duties have been included. It is intended to provide guidelines for job expectations and the employee's ability to reputed company the position described. It is not intended to be construed as an exhaustive list of reputed company functions, responsibilities, skills, and abilities. Additional functions and requirements may be assigned by supervisors as deemed appropriate. This document does not represent a contract of employment, and the company reserves the right to change this job description and/or assign tasks for the employee to reputed company, as the company may deem appropriate. Disclaimer By attaching your Curriculum Vitae (CV), resume, and/or completing an online application, you are consenting to the collection, processing, use, transfer (including but not limited to other countries/jurisdictions), storage, and disclosure of your personal data as described in the Med Communications, Inc. Privacy Policy. Please read this policy carefully for more information on your rights regarding personal data protection. We are an equal opportunity employer and reputed company qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national reputed company, age, disability, genetic information, or veteran status. Recruitment Agency Notice: Thank you for your interest in working with Med Communications. We kindly ask that recruitment agencies avoid sending unsolicited reputed company, as our in-house team manages reputed company hiring processes. Please be aware that any unsolicited reputed company or candidate profiles received without prior engagement or agreement with our recruitment team will be considered free and carry no obligation on the part of Med Communications. We thank you for your compliance with our policy. Should collaboration opportunities arise, we will reputed company out to preferred partners proactively. Your understanding and cooperation are appreciated. Apply To This Job