Senior Data Manager (m/f/d) - Greece

🎯 Who are we?Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients’ lives.Optimapharm’ s key priorities are the well-being of our people, consistent quality delivery to our clients and healthy, sustainable growth.With 26 strategically located offices, Optimapharm operates in 40+ countries, providing most optimal access to Patients and Investigators globally. Established nearly 20 years ago, we leverage our experience, stable project teams and collaborative, and flexible approach to secure a high level of repeat business, gain the trust of new customers and secure continued growth of the company.As a Senior Data Manager at Optimapharm, you’ll be at the forefront of driving data excellence in clinical research. You won’t just manage data; you’ll lead projects, guide teams, and shape the standards that ensure our studies deliver reliable, meaningful results. Partnering closely with cross-functional experts, you’ll play a critical role in transforming complex clinical data into insights that advance science, support our sponsors, and ultimately improve patients’ lives worldwide.🎁 What do we offer?Working in a successful company that’s growing and developing every dayWorking with a highly experienced team of the clinical research professionalsInternational projects and professional growthPerformance bonusReferral bonusPrivate Health CareWork from home daysFlexible work hoursEmployee engagement programsWell-being initiativesTraining and development program🔎 Who are we looking for?💼 Qualifications And ExperienceBachelor’s or higher degree in a biomedical or technical field (e.g., Biology, Biostatistics, Bioinformatics, Engineering) or equivalent industry experience5+ years of proven experience in Clinical Data Management within CRO, pharma, or biotech settings.Knowledge of GCP and ICH GuidelinesExperience in implementing process or technology improvements; experience in supporting business development activities is an advantageStrong understanding of quality systems and regulatory complianceProficient in EDC systems and database standards (e.g., SQL); knowledge of programming languages such as Python, R, SAS, or VBA is an advantageExcellent analytical, organizational, and problem-solving skillsEffective communicator and team player with the ability to manage multiple projects and deadlines📑 Your responsibilitiesLead and oversee end-to-end data management activities across assigned clinical studiesEnsure data accuracy, integrity, and compliance with study protocols and regulatory standardsDevelop, review, and maintain key data management documents (DMPs, CRFs, edit checks, transfer specs)Design, test, and validate EDC systems and related databases, including user acceptance testingManage and coordinate data cleaning, reconciliation, and database lock activitiesPerform and oversee medical coding of adverse events and medications using standard dictionariesAct as the main point of contact for sponsors, vendors, and internal project teamsProvide leadership, guidance, and mentorship to data management team membersParticipate in audits, inspections, and quality improvement initiativesMonitor project timelines, deliverables, and KPIs, ensuring on-time and within-budget deliveryContribute to process harmonization, SOP development, and adoption of best practicesStay current with industry trends, technologies, and regulatory updates in clinical data managementBy joining our fast-growing and prosperous team, you will have a great opportunity for further personal growth and career development. If you would be interested in joining the Optimapharm team, please send your CV in English and note that only shortlisted candidates that meet the requirements will be contacted for the further selection process.Compensation is competitive and final offers will reflect each candidate’s experience, skills, and qualifications.Disclaimer: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.