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OKTO PAYMENTS
Posted: 10/3/2026Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research project management, including sample management, data processing, and compliance with regulatory requirements. Proficient in programming languages and tools for data aggregation and analysis, with strong communication skills to liaise with stakeholders and cross-functional teams.
Highest-signal resume keywords
Clinical Research ExperienceProject Management SkillsKnowledge of ICH and GCP GuidelinesProficiency in Python, R, SQLFluent in English
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Work closely with Precision Medicine Leadership and cross-functional study teams to ensure quality samples and data are managed to support biomarker and non-biomarker evaluation
- Provide project management oversight for sample tracking, usage, collection, destruction and data processing in alignment with protocols and regulatory requirements
- Participate in cross-functional study team meetings and workstreams supporting precision medicine strategy
- Serve as subject-matter expert on sample management and testing, anticipating challenges, managing project risks and responding to stakeholder queries
- Develop and review sample-related sections of clinical protocols, Informed Consent Forms and sample management guidelines
- Support specialty laboratory database creation and validation for data collection and sample kit tracking
- Manage biosample process planning and execution, including storage, shipping and data transfer
- Oversee acquisition and testing of clinical trial samples for biomarker research and liaise with vendors and stakeholders
- Forecast operational costs and timelines; manage budgeting, invoicing and reporting
- Coordinate with data management and biostatistics leads on biomarker data capture, blinding, transfer and reporting
- Develop and review data transfer specifications and related documents
- Train clinical teams and investigative sites on biospecimen collection, storage and shipment compliance
- Ensure human sample transfers are documented, tracked, used and destroyed according to SOPs and regulations
- Potentially lead clinical trial supplies and logistics, including sample and kit inventories, logistics, vendor management, documentation and LIMS tracking
- Support precision medicine logistics strategies and evaluate emerging technologies and vendors
- Potentially lead programming for clinical supplies and laboratory operations, developing tools and dashboards
- Use technical tools, systems and programming languages to aggregate, extract, process and assess data
- Assess laboratory databases, resolve biomarker data queries and support database lock activities
- Complete required training, timesheets, expense reports and CV updates
- Maintain effective relationships across platform lines, business/research units and enabling lines
Requirements
What you’ll need- Candidates must be based in Argentina
- Minimum of 6 years clinical research experience with academic, Contract Research Organization, pharmaceutical or biotech industry
- Working knowledge of clinical drug development process and clinical databases
- Knowledge of ICH, GCP guidelines, and US FDA and/or local country regulations as applicable
- Bachelor degree in life sciences or equivalent (i.e., science, technology, engineering, or mathematics) or relevant work experience
- Biology or equivalent major preferred
- Strong project management and organization skills in a matrix environment
- Analytical and problem-solving experience
- Excellent written and verbal communication skills
- Effective communication and interpersonal skills, with proven ability to build relationships internally and externally
- Fluent in speaking/writing English
- Proficiency in Microsoft Office applications, including strong Excel knowledge, as well as relevant role specific systems
- Proficiency in Python, R, Perl, SQL or other programming languages, familiarity with APIs and Linux/Unix environments, if acting as programming lead for supplies and laboratory operations
Benefits
Comp & perks- No explicit benefits or compensation extras stated
- Full-time employment
- Travel not expected but may occur periodically
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ManagementSample ManagementData ProcessingBudgeting and InvoicingBiomarker Data CaptureAnalytical SkillsProblem-SolvingDatabase ValidationTechnical Tools ProficiencyRegulatory Compliance
Soft Skills
Excellent Communication SkillsInterpersonal SkillsRelationship BuildingOrganizational SkillsTeam Collaboration
Tools & Technologies
Microsoft OfficeExcelLIMS TrackingAPIsLinux/Unix Environments
Industry Keywords
Precision MedicineBiomarker ResearchClinical ProtocolsInformed Consent FormsContract Research OrganizationPharmaceutical IndustryBiotech IndustryClinical Drug Development ProcessSample Kit TrackingHuman Sample Transfers