Digital Health Technology Associate Manager
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Role details
Tech stack
Job description
- Lead the implementation of digital health technologies for clinical research studies from startup through closeout.
- Manage study timelines, project plans, and deliverables for digital technology initiatives.
- Coordinate User Acceptance Testing (UAT), study specifications, translations, and system documentation.
- Collaborate with cross-functional teams, CROs, and external vendors to ensure successful study execution.
- Review and approve project-related documentation throughout the study lifecycle.
- Monitor vendor performance, identify risks, perform root cause analysis, and implement corrective actions.
- Support protocol development related to digital tools and patient technologies.
- Manage licensing, purchasing, and deployment of digital health solutions.
- Track project risks, issues, budgets, and study milestones while providing regular status updates.
- Facilitate issue resolution between internal teams and technology vendors.
- Contribute to process improvements and study-level lessons learned.
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Ensure compliance with ICH/GCP guidelines, SOPs, and regulatory requirements., ePRO eConsent Wearables Sensors Spirometry ECG CTMS
- Are you familiar with ICH/GCP guidelines and regulatory requirements for clinical trials?
Requirements
Do you have experience in Vendor relationship management?, Do you have a Bachelor’s degree?, We are seeking an experienced Digital Health Technology Associate Manager to support the implementation and management of digital tools and technologies across clinical research studies. The ideal candidate will have experience with digital health platforms, clinical trial technologies, vendor management, and project coordination while ensuring compliance with ICH/GCP guidelines and internal quality standards., * Bachelor’s degree or equivalent experience.
- 6+ years of experience in Clinical Research, Biotechnology, Pharmaceutical, or CRO environments.
- Experience implementing digital health technologies such as:
- eCOA
- ePRO
- eConsent
- Wearables
- Sensors
- Spirometry
- ECG
- Remote Patient Monitoring technologies
- Strong project management and organizational skills.
- Experience with vendor management and cross-functional collaboration.
- Knowledge of ICH/GCP guidelines and clinical trial processes.
- Experience with User Acceptance Testing (UAT), study startup, and study closeout activities.
- Proficiency with Clinical Trial Management Systems (CTMS) and Microsoft Project/Office Suite.
- Excellent verbal and written communication skills.
- Ability to manage multiple priorities in a fast-paced environment.
Preferred Qualifications
- Experience supporting global clinical studies.
- Familiarity with eClinical platforms and digital patient engagement technologies.
- Strong analytical, problem-solving, and negotiation skills.
- Experience managing budgets and project financials., * How many years of experience do you have working in Clinical Research, Pharmaceutical, Biotechnology, or CRO environments?
- Do you have hands-on experience implementing Digital Health Technologies in clinical trials (e.g., eCOA, ePRO, eConsent, wearables, sensors, spirometry, ECG)?
- How many years of experience do you have managing Digital Health Technology or eClinical projects?
- Have you managed external vendors supporting digital technologies or clinical trial systems?
- Do you have experience conducting User Acceptance Testing (UAT) for clinical technology platforms?
- Which of the following technologies have you worked with? (Select all that apply)
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