Thermo Fisher Scientific

Research Analyst

• Performs and coordinates all aspects of the clinical monitoring and site management process.
• Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation.
• Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.).
• Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.
• Ensures audit readiness.
• Develops collaborative relationships with investigational sites.
• Monitors investigator sites with a risk-based monitoring approach.

Clinical Research Associate – FSP Oncology, Resp, Gen Med, Vaccine

Project Manager

• Serves as the primary contact and lead between the sponsor and the organization at the project level.
• On projects where the scope requires, ensures clear delineation in responsibilities and communication pathways for secondary project leads.
• Drives and owns the overall delivery of the cross-functional project (time, cost, quality).
• Ensures financial stewardship at a project level by demonstrating an intimate understanding of the contract, resource alignment to budget, management of Out of Scope activity, drive the Con Mod process/negotiations and team execution to timelines.
• Establishes, communicates and manages customer expectations to achieve optimal delivery during the project.
• Drives Risk Identification and Issue Resolution at project level (RBQM/RESOLVE).
• Ensures project team compliance with organization policies, SOPs, ICH-GCP, regulatory and project specific requirements.

Senior Project Manager – Neurosciences, Rare Diseases, CAR-T

Data Engineer

• Drive the execution and adoption of the process data analytics (PA) technologies and capabilities for the Biologics (BIO) business unit (BU).
• Build and maintain Discoverant product hierarchies for global BIO programs according to standard best practices for manufacturing process modelling and nomenclature under a formal SDLC change control process.
• Partner with global and site MSAT to build and deliver user requirements and streamline the execution of Continued Process Verification (CPV), routine process monitoring, and external data sharing activities through usage of Discoverant.
• Develop and integrate data visualization solutions into existing MSAT workflows including manufacturing process and material genealogy use cases.
• Work collaboratively to engage site leadership and technical SMEs to advance programs related to global process analytics.
• Liaise with Global IT, Computerized Systems Validation (CSV), and Data Engineering and Process Analytics (DEPA) to adhere to Discoverant platform-level best practices and procedures and provide input for future system enhancements and upgrades.
• Investigate the applicability of advanced analytical tools such as real-time multivariate process modelling or process knowledge management for improving development and manufacturing.
• Support or lead projects related to Pharma 4.0, AI/ML, and other digital transformation initiatives for the BIO BU.

Financial Planning and Analysis

• Financial leader for the BTO and Strategy functions
• Perform return on investment analysis and justifications for manufacturing site investment and cost reduction projects
• Includes financial modeling to ensure appropriate prioritization
• Partner with appropriate leaders and functional areas to develop cases and drive project financial approval processes
• Develops and applies proactive, early indicator reporting metrics to communicate financial risk or opportunities in a timely manner to senior management
• Improve tools to run business; identify, communicate, recommend, and implement corrective actions
• Implementation and oversight of control, process standards, accounting principles, policies and reporting practices
• Partners with leaders to solicit feedback for step level improvements in reporting and continuously make process and system improvements to drive efficiency and productivity
• Drive continuous improvement with the financial analysis and reporting within BTO and Operations Finance
• Lead budgeting, forecasting, and financial activity for responsible functions
• Build upon vision to elevate operations finance as a best-in-class organization by completing both the personnel and operational improvement road map
• Be a dedicated leader
• Train and develop staff
• Implement new programs via coaching and mentoring that improve finance and operations team members performance and efficiency

Senior Finance Manager

Communications

• Contribute to crafting and delivering impactful stories that connect colleagues to our Mission of making the world healthier, cleaner and safer
• Develop and implement comprehensive communications strategies that engage employees across all levels of the organization
• Focus on reaching diverse audiences including manufacturing teams and those with limited computer access
• Work with senior business leaders to translate complex business strategies and scientific innovations into compelling narratives
• Manage multi-channel communications campaigns that highlight customer success stories, product launches, and organizational initiatives
• Foster an inclusive culture of engagement and recognition
• Collaborate with communications colleagues on company-wide initiatives
• Guide creative storytelling efforts and support employee engagement through various channels including town halls, digital platforms, and leadership communications
• Serve as a key partner in change management initiatives and organizational transformations, ensuring clear and effective message distribution throughout the organization.

Strategic Communications and Organizational Change Manager

Program Manager

• Client facing role responsible for managing the client relationship and on time delivery of program objectives.
• Oversees the coordination and management of a program by monitoring program/project status, adhering to timelines and budgets.
• Acts as the primary liaison between the client, business development, and the project team facilitating the flow of information between all parties.
• Works closely with laboratory management to ensure that the project deliverables meet customer expectations and financial commitments.
• Negotiates and makes real-time decisions with the client.
• Drives compliance to company and project management standards across departments for a cohesive customer experience.
• Provides internal consulting on project management issues and identifies opportunities for process and efficiency improvement.
• Acts as chief liaison to the operational personnel of major clients and is responsible for large study programs.
• Coordinates client visits in tandem with Business Development and Lab Operations management.
• Supports/Leads program governance model.
• Oversees complex stability launch coordination.
• Responsible for the FTE project management, including setup, monitoring and completion.

Program Manager III – Small Molecule, GMP

Product Manager

• Lead the strategy, vision, and execution of flagship digital capabilities supporting the Analytical Services Division within the Clinical Research Group
• Align product roadmaps with business objectives, customer needs, and regulatory requirements
• Translate complex laboratory, operational, and business requirements into detailed product specifications, features, and user stories
• Partner closely with engineering, UX/UI, lab operations, quality, and scientific stakeholders to ensure precise execution
• Lead agile product development cycles, ensuring clarity of requirements, rapid iteration, and high-quality delivery
• Represent ASD product needs within the broader CRG Digital organization and ensure alignment across shared platforms
• Collaborate effectively with data scientists and ML engineers; demonstrate fluency in AI/ML concepts (e.g., regression, classification, NLP, predictive modeling) and their application in laboratory and clinical contexts

Director, Digital Product Manager, Analytical Services

Clinical Research

• Join our Clinical Research team as a Principal Biostatistician where you'll contribute to advancing life-changing therapies through statistical excellence
• Work closely with clients while utilizing the benefits and resources of an established leader in clinical research
• Responsible for implementing diverse statistical tasks throughout the full clinical trial process, from study design and protocol writing to final analysis and reporting
• Opportunity to impact health outcomes while working with advanced clinical development programs

Principal Biostatistician

• Manage a portfolio of Commercial Supply Agreement customers, ensuring smooth post-execution support by collaborating with internal cross-functional teams, coordinating purchase orders, inventory, supporting documentation for order release holds on orders, and managing the regular customer-facing order review meetings
• Serves as the internal link between departments, maintaining direct communication with both internal stakeholders and external customers
• Initiates the involvement of appropriate internal teams, maintains ongoing communication and ensure deliverables meet company and customer standards
• Work under the direction of the Strategic Alliance Manager, to review and align quarterly forecasts and support annual price notification activities as required
• Collaborate effectively with the global team- including Operations, Logistics, LCS Customer Service and other key partners-to address customer needs and resolve issues efficiently
• Coordinates inventory review for single lot availability, and coordinates with internal partners to secure inventory not yet available for production or shipment
• Performs other related duties as the need arises and/or assigned

Client Services Project Manager, Cell Gene Therapy

Field Engineer

• Provide on-site professional technical support, primarily in Hillsboro, Oregon.
• Develop innovative solutions to customer challenges.
• Support tool acceptance and new technologies on location and in coordination with the product and service teams.
• Develop positive relationships with our customers as the technical partner for solving their challenges, explaining our technology, and assisting with application development.
• Coordinate closely with internal product, engineering, marketing and account teams on product acceptance and development.
• Provide detailed technical feedback to the product teams on customer needs and product performance in the field.

Field Applications Engineer, Semiconductor

Director

• Lead innovative diagnostic and life science solutions that help improve healthcare outcomes
• Direct cross-functional R&D teams developing advanced products while fostering a culture of innovation and excellence
• Create compelling technology roadmaps, lead innovation initiatives, and drive new product development from concept to market launch
• Collaborate across business units, manage external partnerships, and ensure alignment with industry regulations and quality standards

Senior Director, Research and Development

Sales

• Drive eBusiness revenue growth and enhance customer experience.
• Lead the development and execution of the regional eBusiness strategy across EDI Integration, Webshop, and Hosted Catalogues.
• Collaborate closely with Sales, Product Management, Marketing, and internal teams.
• Drive customer onboarding and manage communication between stakeholders.
• Develop pricing strategies and ensure consistent achievement of ePO and revenue growth targets.
• Deliver training programs and provide subject matter expertise to support all eBusiness channels.

eSolutions Sales Specialist

Manager

• Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP.
• Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan.
• Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents.
• Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central).
• Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
• Collaborate with the clinical team and other departments as needed to meet deliverables of the project.
• Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained.
• Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies.
• Responsible for the timely archiving of documents and study materials for the department.
• Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics.
• Provide status updates to the project manager, regularly reviewing projects using tracking and management tools.
• Continuously monitor or co-monitors clinical trials to assess performance and ensure contractual obligations are met.
• May communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
• May coordinate all start-up activities and ensures that timely ethics committee and regulatory submissions (if appropriate) are addressed.
• Ensure that essential document quality meets the expectation of Regulatory Compliance Review.
• May provide input into preparation of forecast estimates for clinical activities.
• Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.

Senior/Principal Clinical Team Manager – Neuroscience

• Lead and/or contribute to internal planning meetings, training calls, client KOM and interim client teleconferences
• Collaborate on the development of initial site list development (initial site prioritization)
• Ensure accuracy and quality of survey driven data, including review and QC of departmental deliverables at all stages of the feasibility conduct
• Review and analyze project status to ensure successful completion of milestones, timelines and deliverables
• Serve as the primary point of contact for the department and liaise cross-functionally
• Work with team to identify potential risks and out of scope activity; discuss contingency plans with strategist and/or PM; identify risk trends across projects
• Contribute to the development of best practices for feasibility conduct
• Contribute to the development, testing and maintenance of the electronic survey tool
• Ensure compliance with departmental training plans and required SOP/WPDs
• Assist in the development of the feasibility budget in the instance of budget modification. Manage feasibility hours / budget for assigned projects
• May act as support for senior team members on larger and/or key client projects.

Associate Feasibility Manager

Engineer

• Design and optimize clinical prompt templates
• Conduct structured prompt experiments
• Translate experimental findings into production-ready configurations
• Operationalize prompt updates using Git and Azure DevOps
• Develop and maintain Python/Linux research scripts
• Incorporate feedback into structured rollout plans
• Define monitoring strategies and evaluation criteria