Technical Project Manager

Premium Health is seeking a highly organized and collaborative Technical Project...

Location

United States , Brooklyn

Salary:

110000.00 - 130000.00 USD / Year

Premium Health

Expiration Date

Until further notice

Requirements

Bachelor’s degree in information technology, Computer Science, Healthcare Informatics, or related field
3+ years of experience in IT project management, preferably in a healthcare or nonprofit setting
Excellent communication skills, with the ability to translate technical details for non-technical stakeholders
Strong organization, time management, and prioritization abilities
Critical thinking, problem-solving, and conflict resolution skills
Adaptability and comfort managing multiple concurrent projects in a fast-paced environment
Strong customer service mindset, with focus on supporting clinical and operational needs
Ability to lead cross-functional teams and build consensus across departments
Proficiency with project management tools (e.g., MS Project, Wrike, Asana, Jira, Trello)
Basic understanding of networking, cloud, security, or database environments

Job Responsibility

Coordinate the planning and execution of end-to-end project activities for IT initiatives, including scope definition, scheduling, budget tracking, and resource allocation in collaboration with IT leadership
Collaborate with internal IT staff, department stakeholders, and external vendors to ensure timely and successful project delivery
Translate stakeholders’ needs into clear technical requirements, project plans, and roadmaps
Support project budget tracking by gathering cost estimates, tracking expenditures, and coordinating procurement activities, ensuring adherence to purchasing policies
Assist with vendor selection, contracting, and procurement processes to support project goals
Support project intake and triage by reviewing incoming IT requests, clarifying scope and requirements, and coordinating prioritization with IT leadership and stakeholders
Monitor project progress, identify risks, and implement mitigation strategies
Review and analyze helpdesk metrics to identify trends, recurring issues, and opportunities for workflow or system improvements, and collaborate with IT leadership to prioritize enhancements
Conduct workflow and business process analysis with clinical, administrative, and operational departments to understand current processes and identify opportunities for IT-driven improvements
Develop and maintain project documentation, such as charters, timelines, status reports, and post-implementation reviews

What we offer

Public Service Loan Forgiveness (PSLF)
Paid Time Off
Medical, Dental and Vision coverage with MERP
403(b) Retirement plan with employer matching contribution

Fulltime

Sr. Project Manager - Mobile App

The Sr. Project Manager – Mobile App will lead strategy, planning, and execution...

Location

United States , Burlington

Salary:

130000.00 - 140000.00 USD / Year

Myomo

Expiration Date

Until further notice

Requirements

Bachelor’s Degree required
degree in Engineering, Computer Science, or related technical field preferred
5+ years of project management experience with a focus on software or digital health products, ideally within the medical device or regulated industry
Proven experience in mobile app development and launch, including oversight of agile or hybrid software development processes
Experience working with cross-functional teams in a matrixed environment
Familiarity with FDA, ISO 13485, IEC 62304, and other medical software development standards
Strong organizational, communication, and problem-solving skills
Experience integrating hardware and software systems (e.g., Bluetooth-enabled medical devices)
PMP Certification preferred

Job Responsibility

Lead the development and launch of a mobile app that integrates with existing and next-generation Myomo orthotic devices
Manage all aspects of mobile software project planning and execution including schedules, risk management, milestones, and budgets
Collaborate cross-functionally with software engineering, hardware, regulatory, quality, marketing, and clinical teams to ensure product requirements and compliance needs are met
Drive execution through the phase gate process, ensuring adherence to design controls and software quality system requirements
Facilitate cross-departmental communication and ensure stakeholder alignment
Contribute to resource planning, project cost estimation, and forecasting in alignment with PMO and business priorities

Fulltime

Technical Support Transplant Europe – Clinical Marketing

This role combines advanced technical application expertise with strong clinical...

Location

Spain

Salary:

Not provided

werfen

Expiration Date

Until further notice

Requirements

Advanced degree in Biomedical Sciences, Immunology, or related field
specialization in HLA / histocompatibility / transplant highly preferred
Minimum 5 years of experience in the IVD, transplant, or immunogenetics field, ideally in roles combining clinical, technical, and marketing responsibilities
Deep understanding of transplant diagnostics, HLA typing, antibody testing, and related workflows
Strong knowledge of clinical applications, assay interpretation, and lab operations
Experience with health economics, clinical evidence generation, and case study development is a plus
Proficient in complaint management systems and customer satisfaction testing
Excellent communication and relationship-building with clinical and scientific stakeholders
Ability to translate complex clinical and technical concepts into value-driven marketing and training strategies
Strategic thinker with operational agility

Job Responsibility

Act as second-level technical, scientific, and application support for the Transplant portfolio across all European affiliates
Manage complaint and non-complaint cases for all products within the Transplant portfolio
Provide technical assistance to support the completion of sales processes
Initiate and monitor corrective and preventive actions (CAPAs)
Maintain continuous communication with affiliates
Enhance customer support excellence by promoting best practices
Contribute to User Acceptance Testing (UAT) for new product releases
Provide clinical expertise and strategic guidance on the integration and use of Transplant solutions
Work closely with KOLs, affiliates, Scientific Affairs and Market Access to design and coordinate clinical studies
Establish, strengthen, and expand relationships with Key Opinion Leaders (KOLs) and scientific societies

Fulltime

Manager, CSAR - Global Library

The Global Library Manager will report to the Sr. Manager, Clinical System and A...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree in life science, computer science, business administration or related field and 4 to 6 years of experience
Bachelor’s degree in life science, computer science, business administration or related field and 6 to 8 years of experience
Diploma in life science, computer science, business administration or related field and 10 to 12 years of experience
Broad knowledge / work experience in data management / programming in the Pharmaceutical or Biotech arena
General project management and planning experience
Experience in oversight of outside vendors (CRO’s, central labs, imaging vendors, IRT vendors, etc.)
Good Clinical Practice knowledge
Strong understanding and experience in the use of performance management techniques, measures, problem-solving and analytical thinking
Knowledge of drug development and clinical trials processes
Knowledge of data management processes

Job Responsibility

Support of clinical trial platform technologies
Support decision-making by acting as a data scientist bringing awareness to patterns and analytical insight
Leading and / or coordinating the definition of studies in clinical trial databases or clinical systems
Coordinating and providing programming support to Clinical Study Teams
Maintaining standard business processes within GDO to ensure compliance to regulatory bodies
Acting as a technical point of contact for systems deliverables on defined programs
Providing technical and business process input / expertise on new and emerging technologies
Develop, review and implement policies, SOPs and associated documents
Assist in preparing for and responding to audit findings (internal or external)
Provide Global Library review at the study level

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Clinical Systems Leader

The Clinical Systems Leader (CSL) is responsible for implementing all related cl...

Location

United States , South San Francisco

Salary:

Not provided

Revel IT

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in life science, computer science, engineering, information system, data science or related discipline
2-5 years of experience in Clinical Operations, or Clinical Systems Management
2-5 years of IxRS/IRT and clinical-related systems experience
Successful track records in leading the implementation of clinical systems, such as IxRS/IRT, ePRO, and eCOA
Working knowledge of Good Clinical Practices and FDA regulations governing clinical trial execution
Excellent written and verbal communication skills and strong project management skills
Familiar with documentation in a regulated environment

Job Responsibility

Implement all related clinical systems actions used in the development of clinical trials within Early Clinical Development (ECD)
Collaborate with a cross-functional team of internal stakeholders and technology vendors to ensure the successful implementation and maintenance of technology solutions supporting clinical trials
Focus on system build, vendor selection, specification finalization, and providing UAT oversight
Interpret study protocols, define requirements, work with vendors to build the system, and perform project and vendor management
Accountable for implementing all related clinical systems, such as Interactive Response Technologies (IxRS) and electronic Clinical Outcome Assessments (eCOA) actions for the ECD portfolio
Closely manage study-related timelines and associated activities
Manage and lead the end-to-end specifications for the build of clinical systems for an assigned study or enterprise project
Provide technical oversight to ensure that clinical systems solutions adhere to the study protocol, industry regulations/best practices, and company policies, procedures, and guidelines
Work with a cross-functional team of internal stakeholders and technology vendors
Proactively identify and track study-level technical issues to resolution

New

Project Specialist

As a part of the global Project Leadership group at Parexel, you are responsible...

Location

India , Bengaluru

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Initial years of experience in a similar role preferred
Extensive working knowledge of the English language
Bachelor’s degree in a science-related field, with an advanced degree desirable
PMP or equivalent desirable

Job Responsibility

Project Initiation Management: Ensures tools are set-up according to SOPs and work instructions
Setup of Project Specific Training in LMS
Works with PL to create an initial schedule and resource plan
Assists with drafting a consistent and coherent project management plan
Project Execution and Control Management: Responsible for reporting and analysis and for highlighting issues for project team
Maintains the project schedule and resource changes
Prepares portions of the monthly management and dashboard reports
Updates and maintains project tracking databases
Organizes incoming and outgoing correspondence for project management
May be responsible for managing project document storage

What we offer

Supportive work environment
High degree of empowerment and accountability
Work with a diverse set of clients and therapeutic areas
Encouraged to take on new challenges and pursue your interests
Supportive and inclusive environment
Flexible work arrangements: remote, in-office and hybrid roles
Varied project experience
Career progression

Fulltime

Clinical System Designer

Clinical System Designer - India. ICON plc is a world-leading healthcare intelli...

Location

India , Bangalore

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Uses technical, industrial, and interpersonal skills, with some support from project team leads and their people leader, to interpret clinical protocols and customer requirements in order to create clinical data management system (CDMS) designs and non-CDMS component specifications (including electronic Case Report Forms (eCRFs), dynamic eCRF functionality and eCRF edit checks) to meet the needs of the customer and the clinical trial
Responsible for optimal design decisions and the utilization of ICON/client specific standards
Good functional knowledge of at least one clinical data management system and CRF design tool
Ability to plan and design CDMS components directly from interpretation of low to medium complexity clinical trial protocols
Acts as first point of contact during study build for assigned projects for design related questions by the project team
Read, ensure understanding and adhere to the study protocol, contract and scope of work for all task during set-up, maintenance and close-out of the study
Tracks and keeps functional management and those responsible for project management informed of any issues that might affect project target dates, scope or budget and escalates potential problems effectively and in a timely manner
With support, consolidates and completes the high-level system requirements documents and facilitates their review
Assumes responsibility for copying and modifying CRFs from standard libraries and other studies
Assumes responsibility for development of Custom CRF screens, Edit Check and Dynamic Check specification documents, using prototyping methodologies as needed

Job Responsibility

Uses technical, industrial, and interpersonal skills, with some support from project team leads and their people leader, to interpret clinical protocols and customer requirements in order to create clinical data management system (CDMS) designs and non-CDMS component specifications (including electronic Case Report Forms (eCRFs), dynamic eCRF functionality and eCRF edit checks) to meet the needs of the customer and the clinical trial
Responsible for optimal design decisions and the utilization of ICON/client specific standards
Good functional knowledge of at least one clinical data management system and CRF design tool
Ability to plan and design CDMS components directly from interpretation of low to medium complexity clinical trial protocols
Acts as first point of contact during study build for assigned projects for design related questions by the project team
Read, ensure understanding and adhere to the study protocol, contract and scope of work for all task during set-up, maintenance and close-out of the study
Tracks and keeps functional management and those responsible for project management informed of any issues that might affect project target dates, scope or budget and escalates potential problems effectively and in a timely manner
With support, consolidates and completes the high-level system requirements documents and facilitates their review
Assumes responsibility for copying and modifying CRFs from standard libraries and other studies
Assumes responsibility for development of Custom CRF screens, Edit Check and Dynamic Check specification documents, using prototyping methodologies as needed

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Fulltime

Quality Management Specialist

We are providing a contract for a fulltime employment opportunity for a Quality ...

Location

United States , Oakland

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Possess strong management skills with the ability to oversee multiple tasks simultaneously
Proficiency in reporting and analytics, with a keen eye for data analysis and metric reporting
Demonstrated experience in strategic planning and implementation
Familiarity with drafting, interpreting, and implementing procedures and policies
Solid understanding of quality design and optimization principles
Knowledge in project management and the ability to handle multiple projects simultaneously
Excellent presentation skills with the ability to communicate complex information effectively
Must provide medical coverage knowledge and demonstrate understanding of clinical trial operations
Strong leadership skills, with the ability to inspire and motivate a team
Consulting experience, with the ability to provide expert advice and guidance

Job Responsibility

Lead the planning, coordination, and monitoring of clinical care and outcomes improvement strategies
Coach and consult individuals, departments, and multi-disciplinary teams on quality improvement processes and tools
Analyze existing care delivery models to identify opportunities for systems-based improvements
Oversee reporting requirements, establish guiding metrics, and benchmarks for performance improvement initiatives
Collaborate with medical information teams to design safe, high-quality workflows
Develop presentations to disseminate information and updates on improvement strategies
Facilitate and sustain performance improvement initiatives and activities in the healthcare setting
Ensure compliance with regulatory and accrediting agency requirements, maintaining a focus on data integrity, integration, and standardization
Assist in evaluating current and future quality initiatives within the health system
Advocate for best practices in patient safety, quality, and patient experience within the organization

What we offer

medical, vision, dental, and life and disability insurance
eligible to enroll in our company 401(k) plan

Fulltime

Technical Project Manager – Clinical Systems

canfield scientific

Location:
United States of America

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
April 15, 2026

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