CenExel

Product Manager

• The Product Manager is responsible for defining, delivering, and continuously improving healthcare technology products that support clinical, operational, and patient outcomes.
• Working within an Agile development framework, this role collaborates closely with engineering, design, clinical stakeholders, and business teams to translate healthcare needs into scalable, compliant, and user-centered digital solutions.
• The Product Manager owns the product roadmap, prioritizes features, and ensures that product development aligns with regulatory requirements, market needs, and organizational strategy.
• Define and communicate the product vision, strategy, and roadmap for healthcare technology solutions.
• Identify market opportunities and user needs through research, analytics, and stakeholder engagement.
• Align product goals with organizational objectives and healthcare industry trends.
• Maintain and prioritize the product backlog in collaboration with Agile development teams.
• Write clear user stories, acceptance criteria, and product requirements.
• Participate actively in Agile ceremonies including sprint planning, backlog grooming, stand-ups, sprint reviews, and retrospectives.
• Work with clinicians, healthcare administrators, compliance teams, and customers to gather requirements and validate product features.
• Collaborate with UX/UI designers and engineering teams to deliver intuitive, high-quality solutions.
• Ensure products comply with healthcare regulations and standards (e.g., HIPAA, interoperability standards, data security).

Project Manager

• Oversees the planning, execution, and close-out of clinical research studies for single and multi-site studies
• Ensures operational excellence, regulatory compliance, and timely delivery of study milestones
• Leads cross-functional teams through all phases of clinical trial execution
• Develops and manages project timelines and deliverables
• Monitors progress against milestones and proactively addresses risks or delays
• Tracks enrollment metrics, protocol deviations, and site performance
• Optimizes resource allocation and capacity planning
• Coordinates with sponsors, CROs, and internal teams to ensure alignment
• Maintains Trial Master Files (TMF)
• Supports audit readiness and CAPA implementation

Research Analyst

• Monitors clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Conducts site selection, initiation, monitoring, and close-out visits.
• Reviews case report forms (CRFs) for accuracy and completeness.
• Verifies source documents to ensure data integrity.
• Liaises between sponsors and clinical trial sites to resolve issues.
• Ensures timely reporting and resolution of adverse events.
• Maintains and updates study documentation and records.
• Trains site staff on study protocols and compliance procedures.
• Ensures proper handling and storage of investigational products.
• Prepares monitoring visit reports and presents findings.

Clinical Research Associate

• Oversees the planning, execution, and close-out of clinical research studies for single and multi-site studies
• Ensures operational excellence, regulatory compliance, and timely delivery of study milestones
• Leads cross-functional teams through all phases of clinical trial execution, including study start-up, conduct, and close-out phases
• Develops and manages project timelines and deliverables
• Monitors progress against milestones and proactively addresses risks or delays
• Tracks enrollment metrics, protocol deviations, and site performance
• Optimizes resource allocation and capacity planning
• Serves as primary contact for sponsors and external vendors
• Coordinates with sponsors, CROs, and internal teams to ensure alignment
• Facilitates communication across teams by conducting regularly scheduled team meetings
• Manages project according to Operational Study Plans (Project Management Plan, Monitoring Plan, Clinical Site Blinding Plan, etc.)
• Supports audit readiness and maintains complete, compliant documentation.

Sponsor Research Division Project Manager

Manager

• Manage the full lifecycle of early business capture and operational study start-up
• Integrate proposal development, feasibility analysis, startup oversight, and sponsor-facing communication
• Ensure proposals are competitive and accurate
• Conduct feasibility assessments across sites
• Develop costing models, timelines, and operational strategies based on protocol requirements
• Maintain proposal templates and a library of historical pricing data
• Lead start-up activities from award through site activation
• Collaborate with investigators, site operations, and sponsors during the feasibility and activation phases
• Ensure documentation is audit-ready and compliant with regulatory standards

Manager, Proposals – Study Start Up

Clinical Research

• Overseeing the feasibility of projects for the organization
• Conduct feasibility studies to help project managers understand all aspects of the project feasibility
• Find potential problems during a project’s implementation
• Determine a project’s viability and define alternative solutions to obstacles
• Manage feasibility studies and supervise assigned staff
• Manage contract negotiations
• Assumes other duties and responsibilities as assigned

Product Manager

Project Manager

Clinical Research Associate

Sponsor Research Division Project Manager

Manager, Proposals – Study Start Up

Feasibility Manager