Orion

Support Engineer

• serve as a technical support resource for Advisor Portal related questions, workflows, and client impacting issues
• respond to Advisor Portal inquiries across phone, email, chat, Salesforce cases, and scheduled consultations
• troubleshoot issues related to proposals, new account opening, account maintenance, client onboarding, trading related workflows, and other Advisor Portal functionality
• support DocuSign related workflows within Advisor Portal, including document generation, envelope routing, signing order questions, advisor and client signing experiences, and troubleshooting related errors
• analyze technical issues, configuration questions, workflow discrepancies, and user reported concerns
• provide clear guidance to advisors, internal service teams, onboarding teams, and other business partners
• follow established training, documentation, procedures, and escalation paths to support consistent and accurate resolutions
• collaborate with Product Management, Development, Service, Onboarding, Operations, and other internal teams on defects, enhancements, workflow changes, and client impacting issues
• act as escalation support for Advisor Portal cases as knowledge and experience grow
• document troubleshooting steps, technical findings, workflow guidance, and best practices
• help improve Advisor Portal enablement, internal documentation, training resources, and support processes
• mentor and support peers over time through shadowing, coaching, and knowledge sharing

Technical Support Specialist

Manager

• Lead and manage environmental responsibility within G-OPS in line with Orion’s EHS policies and applicable regulations
• Develop and manage the G-OPS environmental management system, including ISO 14001-related practices, processes, and ways of working
• Plan, implement, monitor, and continuously improve environmental management operations
• Define environmental objectives, targets, and KPIs, and drive their implementation and follow-up
• Ensure that environmental regulations, standards, and procedures are recognized and implemented across operations
• Drive environmental improvement programs and projects aligned with Orion’s corporate targets
• Collaborate closely with internal stakeholders, including G-OPS management, EHS and Sustainability functions, to establish targets and processes
• Act as the main contact towards relevant authorities and support environmental inspections and audits (e.g. by the Finnish Safety and Chemicals Agency (Tukes))
• Lead the G-OPS environmental management network
• Provide expert support and guidance to sites and stakeholders to foster a strong environmental responsibility culture

Manager, Environmental Responsibility

Procurement

• Take responsibility for sourcing projects within the IM category
• Work closely with suppliers and internal stakeholders
• Collaborate with the IM Category Manager and other key stakeholders
• Plan and lead sourcing cases, including RFIs and RFPs
• Coordinate commercial, technical, risk, and compliance evaluations
• Develop sourcing practices, templates, and capabilities
• Support Supplier Relationship Management (SRM) activities

Sourcing Manager

Data Scientist

• Provide leadership for clinical data management activities across multiple oncology studies and development programs.
• Serve as the senior Data Management representative on cross-functional program teams and contribute to strategic development planning.
• Define and implement data management strategies that support efficient study execution, regulatory compliance, and submission readiness.
• Lead the design and development of eCRFs, database builds, edit checks, derivations, data review plans, and study-level data management documentation.
• Ensure effective integration, reconciliation, and quality oversight of external data sources including laboratory, imaging, ePRO, genomic, biomarker, and safety data.
• Drive data quality initiatives and ensure timely resolution of data issues through proactive review, risk-based approaches, and operational metrics.
• Lead database lock planning and execution activities and ensure delivery of high-quality datasets supporting statistical analysis and regulatory submissions.
• Ensure compliance with CDISC standards, ICH-GCP requirements, applicable regulations, SOPs, and industry best practices.
• Serve as the Data Management representative on regulatory inspections, audits, due diligence activities, and health authority interactions related to clinical data management.
• Drive continuous improvement initiatives, standardization efforts, and implementation of scalable data management processes across the portfolio.
• Lead evaluation and adoption of AI-enabled technologies, automation platforms, and advanced analytics solutions that improve data quality, operational efficiency, query management, and risk detection.
• Establish governance and best practices for responsible use of AI-assisted data review and automated workflow solutions within clinical development.
• Contribute to department strategy, resource planning, talent development, and organizational objectives established by the Head of Clinical Data Management.

Lead Clinical Data Management, Clinical Data Management

Software Engineer

• Independently lead programming activities of moderate to high complexity while ensuring quality, accuracy, and adherence to timelines.
• Develop, validate, and maintain SDTM and ADaM datasets in accordance with CDISC standards, study specifications, and regulatory requirements.
• Program, validate, and deliver Tables, Listings, and Figures (TLFs) for clinical study reports, interim analyses, and regulatory submissions.
• Perform quality control (QC) reviews and ensure traceability, reproducibility, and compliance of programming deliverables.
• Contribute to the development of dataset specifications, define.xml files, reviewer guides, and other submission documentation.
• Support preparation and delivery of electronic submission packages for global regulatory agencies, including FDA and EMA.
• Collaborate with Biostatisticians on implementation of Statistical Analysis Plans (SAPs) and interpretation of programming requirements.
• Support data review, data cleaning, discrepancy management, and database lock activities throughout the study lifecycle.
• Work closely with Data Management and external vendors to ensure consistency of standards and data quality.
• Ensure compliance with SOPs, GxP requirements, CDISC standards, and industry best practices.
• Drive adoption of innovative programming approaches and AI-assisted workflows to improve efficiency, quality, and scalability of clinical trial deliverables.
• Contribute to programming standards, macros, and process improvements that enhance efficiency and quality.
• Provide technical guidance and mentoring to junior programmers when appropriate.

Senior / Principal Statistical Programmer, Clinical Development Data Services

• Provide leadership and oversight for statistical programming activities across multiple clinical studies and development programs.
• Serve as the programming lead for assigned programs and represent Statistical Programming on cross-functional development teams.
• Develop and implement programming strategies that support clinical development objectives, regulatory submissions, and operational efficiency.
• Oversee the development, validation, and delivery of SDTM, ADaM, TLFs, define.xml files, reviewer guides, and other submission-related deliverables.
• Ensure programming deliverables are completed with high quality, on schedule, and in compliance with regulatory requirements and company standards.
• Drive the development, maintenance, and governance of programming standards, tools, templates, and best practices.
• Act as a subject matter expert on CDISC standards, regulatory submission requirements, and programming methodologies.
• Collaborate with Biostatistics to ensure efficient implementation of Statistical Analysis Plans and consistency of statistical deliverables.
• Contribute to submission strategies and support regulatory filings, including NDA, BLA, and MAA submissions.
• Drive continuous improvement initiatives, automation strategies, and adoption of innovative technologies to improve programming efficiency and quality.
• Evaluate and promote appropriate use of AI-assisted development tools, automation frameworks, and modern analytics technologies within the programming environment.
• Mentor, coach, and develop statistical programmers while fostering technical excellence and professional growth.

Statistical Programming Lead, Clinical Data Management, R&D

• Lead all clinical data management activities for one or more oncology clinical studies from protocol development through database lock and study closeout
• Serve as the primary Data Management representative on cross-functional study teams and act as the main point of contact for data management-related activities
• Lead the design, review, and implementation of eCRFs, database builds, edit checks, derivations, and data validation rules in alignment with study protocols and regulatory requirements
• Lead the integration and reconciliation of external data sources including laboratory, imaging, safety, ePRO, genomics, biomarker, and other vendor datasets
• Develop and maintain Data Management Plans, Data Transfer Agreements (DTAs), data specifications, reconciliation plans, and study-level documentation
• Responsible for query management, discrepancy resolution, medical coding (MedDRA, WHODrug), and SAE/PV reconciliation
• Drive database lock planning and execution to ensure timely delivery of high-quality, submission-ready datasets
• Ensure compliance with CDISC standards (CDASH and SDTM), ICH-GCP requirements, SOPs, and applicable regulatory guidance
• Support regulatory submissions, inspection readiness activities, audits, and health authority requests
• Identify opportunities to improve data quality, process efficiency, and operational scalability through automation and standardization initiatives
• Partner with cross-functional stakeholders to evaluate AI-enabled solutions that support automated data review, query prioritization, risk identification, and operational efficiency

Senior Clinical Data Manager, Clinical Data Management

Clinical Operations

• Accountable for the day-to-day operational oversight of clinical trial execution
• Oversee study feasibility activities and site management coordination.
• Monitor site activation performance and ensure site enrollment and data quality.
• Prepare and validate clinical study plans and patient-facing materials.
• Support oversight of CROs and vendors in monitoring and site management.
• Coordinate and track key operational metrics.
• Partner with data management, safety, and regulatory teams for smooth execution of study activities.
• Identify risks and operational issues for timely resolution or escalation.
• Ensure adherence to GCP, protocol, and SOPs in daily execution.

Study Monitoring Lead, Clinical Operations, Oncology Therapy Area

• Provide global leadership for the planning, set up, execution, oversight, and delivery of complex oncology clinical trials from First in Human (FIH) through late phase Ph2/3 registration studies and submission.
• Lead the end to end execution of global Phase I–III oncology studies, including FIH and registration enabling trials, from startup through closeout, to ensure the study is delivered within timelines, budget and with high quality.
• Provide hands-on project leadership in a global, cross-functional setting, including study timelines projection, protocol development support, site selection/activation, vendor management, timeline/budget oversight, risk/issue resolution, and CRO performance management.
• Plan, drive and oversee study start up, site activation, enrollment strategy, patient retention, data quality oversight, database readiness, study reporting and CSR delivery aligned with regulatory strategy submission plans.
• Ensure rigorous vendor oversight, particularly CRO performance (monitoring, data management, labs, imaging, ePRO, etc.).
• Proactively identify operational risks and implement robust mitigation plans. Escalate critical issues and propose solutions to senior leadership.
• Plan and manage study timelines, project site activation, recruitment and readout timelines, including building various scenarios depending on data-driven study outcome assumptions and other requirements.
• Manage clinical trial budgets, forecasting, accruals, and change orders.
• Ensure adherence to ICH GCP, local/global regulations, SOPs, and audit readiness, including respond to audits/inspections, and coordinate CAPA implementation, as needed.
• Partner closely with internal and external stakeholders to deliver integrated milestones.
• Chair global study team meetings, drive team collaboration and ensure clear decision making and documentation.
• Build strong relationships with investigators, global KOLs, and academic partners as required.

Clinical Study Delivery Lead, Global Clinical Operations, Oncology

Clinical Research

• Provide scientific and strategic biostatistics leadership for oncology portfolio
• Contribute to clinical development plans and study designs
• Serve as the lead statistician for development programs
• Ensure delivery of biostatistics outputs in line with timelines and quality expectations
• Provide statistical leadership for regulatory submissions
• Define and standardize statistical methodologies
• Lead adoption of AI-enabled analytics and automation

Lead Biostatistician, Biostatistics, R&D

• Contribute to the design and statistical sections of clinical trial protocols, including endpoint selection, sample size considerations, and randomization approaches.
• Support analyses of predictive, prognostic, pharmacodynamic, and other biomarker data to inform development decisions and patient selection strategies.
• Participate in the integration and interpretation of clinical and biomarker findings to generate actionable insights.
• Plan, prepare, and execute statistical analyses according to SAPs.
• Generate and review tables, listings, and figures (TLFs).
• Ensure statistical deliverables adhere to CDISC standards (SDTM, ADaM).
• Support clinical study reporting and regulatory documents.
• Collaborate with clinical, data management, and programming teams throughout the study lifecycle.
• Contribute to the evaluation and appropriate use of AI-assisted tools, automation, and advanced analytics approaches that enhance statistical efficiency and insight generation.

Senior Biostatistician, Biostatistics, R&D

Therapist

• Discover biomarkers for patient selection, target engagement, and pharmacodynamic (PD) effects
• Drive design, development, validation, verification and implementation of translational and clinical-grade biomarker assays to inform essential clinical research questions
• Ensure biomarker studies comply with GXP and other relevant regulatory standards. Partner with internal collaborators to identify and qualify CROs and other vendors appropriately.
• Explore and apply innovative technologies (e.g., spatial omics, digital pathology) to advance biomarker development
• Characterize targets (expression, stability, heterogeneity) to inform indication and patient selection strategies
• Partnering with internal and external collaborators to develop and apply state-of-the-art in vitro, in vivo and ex-vivo models of oncology and Immuno-oncology to inform indication selection, patient selection, Mechanism of action, Mechanism of resistance and combination strategy
• Lead study design, execution oversight, and rigorous analysis/interpretation of preclinical models to generate insights to support clinical development plan
• Evaluate and implement innovative technologies and platforms that increase rigor, throughput, translational relevance, and decision quality from pre-clinical models

Translational Biology Lead, Oncology Therapy Area

• Lead and own Translational Medicine strategy for oncology programs
• Subject matter expert in solid tumor biology
• Serve as the bridge between discovery research and clinical development
• Ensure translational insights are embedded into study trial design
• Collaborate closely with CDx lead and internal collaborators
• Deliver timely, high-quality biomarker data
• Lead reverse translation from patient data to insights
• Contribute to IND, CTA, and regulatory submissions

Translational Medicine Lead, Oncology Therapy Area

Executive

• Manage the entire export delivery process.
• Handle order processing with efficiency and accuracy.
• Organize transportation logistics for export consignments.
• Maintain effective communication and customer relations related to orders and deliveries.
• Collaborate closely with internal departments (sales, warehouse) and external partners (freight forwarding agencies) to ensure smooth operations

Executive, Logistics OPP

Sales

• Recruitment and development of Sales Specialists (SS)
• Leadership & management of Sales Team towards delivery of sales target
• Coaching and development of selling skills
• Supporting delivery and development of KSM and marketing campaigns
• Motivation and team-building