Data Manager for Clinical Trials

Company DescriptionPSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.Job DescriptionClincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for.Please submit your CV in EnglishResponsibilities will include:Track database set-up, testing, maintenance and data entryCommunicate with clients, project teams and vendors on data management mattersReview study documents, design and develop project specific guidelines and instructionsDesign eCRF, Data Management and Data Validation Plans and test EDC databasesEnsure data entry, follow-up and validation, including manual CRF review and SAE reconciliationCode medical dataTrack and report metrics leading to database lockCoordinate the processing, dispatch and archiving of CRFs/queriesMaintain Clinical Data Management working filesPerform database QC checks, prepare and attend auditsTrain site staff and project teams on CRF completion and data management topicsQualificationsCollege/University degree (Life Science, Pharmacy degree is a plus)Demonstrated experience of managing clinical or medical data in a CRO is a mustFull working proficiency in EnglishExperience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)Proficiency in MS Office applicationsOrganisational and time management skillsAbility to work independently and multi-taskAdditional InformationBase salary range: 34,000 - 52,000 gross annual salary.Actual compensation: The salary offered within the stated range will depend on objective, job-related criteria, including demonstrated competencies, qualifications, and skills relevant to the position.Additional compensation: bonus, incentive plans, and other benefits may apply.SummaryType: Full-timeFunction: AnalystExperience level: AssociateIndustry: Pharmaceuticals