Project physician

Ph3Position Summary /h3 pTo Lead Clinical development of One or more GVGH Vaccine Development Programmes through the design and set-up of GVGH-managed clinical trials. To serve as lead author or key contributor of clinical and epidemiology plan and clinical documents (e.g., clinical trial protocols, reports and publications, integrated clinical documents for regulatory submissions, etc.) and to have medical monitoring responsibility for clinical trials of GVGH vaccine project(s). In order to ensure the high quality and on-time delivery of all clinical data that will allow demonstration of Proof-of Concept of GVGH candidate vaccines in line with the clinical development plan, good clinical practices (GCP), and GSK Vaccines/ GVGH standard operating procedures (SOP). To be a member of the cross functional Safety Review Team coordinated by SERM. /p h3Responsibilities /h3 pWork in a Clinical Development sub-team of clinical and regulatory colleagues (clinical development, clinical operations, biostatistics regulatory associates), and in collaboration with non-CDRA members of the GVGH Project Team(s), with the responsibility to author clinical development plans, design clinical trial protocols, write Investigator Brochures, clinical study reports and publications of the project(s) to high scientific, operational and ethical standards. /p ul liAddress scientific and medical issues related to trials of the project(s) in GVGH. /li liBe responsible (or provide oversight of delegated CRO medical monitoring team) for Medical Data Listing review, ensuring medical consistency within trial and across trials within the project. /li liAs a member of the Safety Review Team, be accountable (through providing oversight if applicable of delegated CRO medical monitoring team) for medical assessment of serious adverse events, adverse events of special interest (AESI’s) and other events occurring during clinical trials and pay attention to potential safety signals. /li liParticipate in individual case safety report compliance activities and take the necessary corrective actions. /li liHandling and/or coordinating studies with human biological samples using GVGH WS/GSK policies. /li liSupport the Senior project physician Lead in representing GVGH in meetings with health authorities and the scientific community, network with thought leaders and international agencies on specific GVGH vaccine related project matters. /li liContribute to creation, review and revision of standards (e.g., SOPs, Work Instructions) on clinical development, regulatory and drug safety activities. /li liMaintain/expand knowledge in vaccines, clinical trial methodology, and drug safety competencies including national and international regulations and Global Safety policies/procedures. /li liServe as the principal liaison to GVGH Safety and Data Management Committees: SRT, Internal Safety Review Committee (iSRC) and Independent Data Monitoring Committee (IDMC). /li liWhere applicable, lead matrix team, to author program strategy, clinical development plans and design clinical trial for governance meetings and ensure consistency of data within program and across projects. Reporting accountability will be to the Senior Project Physician Lead. /li /ul h3Budget, Resourcing and Timing /h3 ul liSupports the clinical team to consistently achieve high standards and attainment of project timelines in global programs. /li liInterfaces with the SDL to ensure milestone realization and resource optimization. /li /ul h3Basic Qualifications Skills /h3 ul liDoctor of Medicine with advanced university degree (Masters or PhD) and Board certification. In order of preference: vaccinology, infectious diseases, global health, pediatrics. /li liAt least 2-3 year experience in industry clinical development and/or drug safety in a pharmaceutical company or 10 years working in a scientific or medical Institution. /li liMedical and scientific knowledge and track‑record in infectious diseases through training and practice and the ability to function independently while supervised with significant experience in clinical development and drug safety in academia or industry. /li liDemonstrated experience and initiative in finding solutions to challenges in the clinical development space in LMICs is a key attribute. /li /ul h3Preferred Qualifications Skills /h3 ul liInnovative problem solving is a desirable requirement due to the need to provide balanced clinical and ethical guidance, particularly in the sites and countries where some of the GVGH clinical trials may take place. /li liStrong clinical leadership and excellent interpersonal and communication skills to work effectively with internal GVGH/GSK project teams, CRO partners, external clinical site teams and international scientific and funding stakeholders. /li liProven ability to interact with tact, respect and cultural sensitivity with diverse stakeholders, including opinion leaders, doctors, patients, health workers and community leaders in LMIC settings. /li liHigh level of impact and accountability for project success in clinical development and drug safety, including independent issue resolution and decision‑making. /li liDemonstrated ability to generate, interpret and communicate complex clinical data, taking end‑to‑end responsibility for results, reporting and scientific dissemination with limited supervision. /li /ul h3What we offer /h3 ul liPermanent contract in a very Inclusive environment /li liFlexible Benefits /li liCompany Healthcare Plan /li liIntegrative pension fund /li liEmployee Assistance Programme /li liPrevention services and vaccination clinic /li liTax assistance /li liLocal nursery agreement /li liPostal service, laundry, shoe repair and tailoring /li liOn Site Gym /li liOn Site canteens and coffee corners /li liFree company bikes and shuttle /li /ul h3Salary /h3 pItalian Salary Range / Fascia retributiva in Italia: EUR 60,000 to EUR 100,000. The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. /p h3EEO Statement /h3 pGSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. /p /p #J-18808-Ljbffr