Associate Technical Project Manager

Position Details

• Title: Technical Project Manager


• Work Location: Acton, MA 01720, United States


• Work Model: Remote - Must be onsite in Acton, MA 1-2 weeks per quarter


• Assignment Type: Contract


• Contract Duration: 6 months + possible extension


• Client Industry: Medical Devices


• Pay Range: $45 -$50/hr. on W2

Job Summary

We are seeking a detail-oriented and collaborative Technical Project Manager to support clinical build and study operations within a healthcare technology environment. The ideal candidate will be responsible for coordinating clinical builds for algorithm updates, managing dependencies and readiness across technical, clinical, and quality teams, and developing repeatable processes to support efficient study preparation and software deployment.

This role will focus on process mapping, documentation, device capabilities across iOS and Android platforms, firmware update mechanisms, clinical software build deployment, cloud surveillance, and cross-functional coordination. The position provides an opportunity to contribute to continuous product development within a regulated medical technology environment.

Key Responsibilities

• Lead cross-functional coordination to deliver clinical builds for algorithm updates, managing dependencies and readiness across teams.
  * Map, develop, and document new clinical-build processes, including phone-reuse setup procedures.
  * Establish and maintain repeatable device capability processes for iOS and Android phones used in clinical studies.
  * Define and document how devices utilize firmware update capabilities, including OTA and FOTA.
  * Develop, update, and maintain procedures, checklists, and supporting documentation required for clinical builds.
  * Create a reusable content library to standardize processes and facilitate reuse across multiple updates.
  * Oversee cloud surveillance and monitoring activities for active clinical studies and ensure issues are promptly addressed.
  * Manage deployment, rollout, and version control of clinical software builds across study environments and sites.
  * Collaborate closely with program leadership to map workflows and develop scalable, repeatable processes to accelerate study readiness.
  * Coordinate effectively across engineering, clinical, quality, and IT functions.

Required Skills & Experience

• Bachelor's degree in a scientific, engineering, IT, or related technical field, or equivalent professional experience.
  * Experience in program or project coordination, ideally within regulated environments such as medical devices or digital health.
  * Familiarity with mobile software development and device management across iOS and Android platforms.
  * Knowledge of OTA and FOTA firmware update procedures and connected device deployment.
  * Strong experience with process mapping and documentation, including SOPs, checklists, and workflows.
  * Proven ability to coordinate and communicate effectively with engineering, clinical, quality, and IT teams.
  * Experience working with cloud-based monitoring systems, dashboards, and surveillance tools.
  * Excellent written communication and organizational skills.
  * Ability to work independently with minimal supervision.
  * Exposure to clinical studies, clinical trials, or regulated product operations is a plus.

Preferred Skills & Competencies

• Prior experience with clinical study processes or regulated product development environments.
  * Familiarity with cloud surveillance and monitoring tools for clinical applications.
  * Experience developing reusable process content and documentation standards.
  * Ability to adapt and implement structured enterprise problem-solving methodologies such as 8D, DMAIC, or equivalent frameworks.
  * Strong cross-functional collaboration and stakeholder management skills.
  * Ability to develop scalable and repeatable processes that improve study readiness and software deployment.

Interview Process

• Initial Round: Virtual interview with the hiring team
  * Additional Rounds: Based on client feedback and interview progression

Additional Information

• Work Model: Remote
  * Onsite Requirement: Must be onsite in Acton, MA 1-2 weeks per quarter
  * Contract Duration: 6 months with possible extension
  * Industry Exposure: Medical Devices / Healthcare Technology environment
  * Location: Acton, MA 01720

If this opportunity aligns with your experience and career goals, I'd love to discuss it further with you. Please reply with your updated resume or let me know a convenient time to connect.

Dexian stands at the forefront of Talent + Technology solutions with a presence spanning more than 70 locations worldwide and a team exceeding 10,000 professionals. As one of the largest technology and professional staffing companies and one of the largest minority-owned staffing companies in the United States, Dexian combines over 30 years of industry expertise with cutting-edge technologies to deliver comprehensive global services and support.

Dexian connects the right talent and the right technology with the right organizations to deliver trajectory-changing results that help everyone achieve their ambitions and goals. To learn more, please visit .

Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.