PHARMAFull-time
Associate Digital Health Technologies Manager
By Admin · IT & Software in Life Sciences
HYDERABAD (IN)REMOTEPOSTED: 9/3/2026
PHARMAFull-time
HIRING ORGANIZATIONPAREXELBiosciences / Healthcare, Contract Research Organization (CRO)
ROLE DEFINITION & RESPONSIBILITIES
Core Responsibilities
Manage implementation of Digital Health Technologies (DHTs) in individual clinical research studies from study design through close-out.
Support technologies including electronic Clinical Outcome Assessments (eCOA), electronic consent (eConsent), wearables, sensors, spirometry, ECG and other digital tools.
Collaborate closely with clinical study teams throughout study execution.
Manage project timelines, translations, specifications and User Acceptance Testing (UAT) activities.
Directly participate in UAT execution or oversee UAT activities, as appropriate.
Ensure digital technology data collection follows Client Standard Operating Procedures (SOPs) and ICH/GCP requirements.
Support both internally sourced studies and studies outsourced to Clinical Research Organizations (CROs).
Manage activities performed by technology and service vendors.
Provide training and education to relevant stakeholders regarding digital health technologies and study processes.
Technical & Regulatory Expertise
Demonstrate knowledge of digital tools and technologies, particularly eCOA system development processes.
Apply knowledge of ICH/GCP and relevant regulatory guidelines and directives to clinical-study technology implementation.
Maintain awareness of relevant Digital Health Technology industry trends.
Possess technical knowledge of trial management systems and Microsoft Project Server.
Project & Vendor Management
Manage multiple concurrent activities and deliverables in a complex clinical-research environment.
Plan, execute and solve problems using a data-driven approach.
Manage vendor activities and maintain effective relationships with external vendors.
Coordinate cross-functional stakeholders and provide leadership throughout technology implementation.
Manage timelines, prioritize work and ensure deadlines are met.
Leadership & Communication
Demonstrate interpersonal and leadership skills when working with internal stakeholders and external vendors.
Communicate effectively through verbal, written and presentation formats.
Understand and apply the strategic direction and guidance established for clinical studies.
Influence stakeholders and negotiate effectively when managing study and vendor requirements.
Work independently while managing multiple priorities and tasks simultaneously.
Demonstrate proactive, self-disciplined and well-organized working practices.
Qualification & Experience
Bachelor's degree required.
Minimum 6+ years of relevant industry experience required.
Relevant experience should support digital health technology, clinical research, project management, vendor management or related clinical-development activities.
Company Context
Parexel operates across clinical trials, regulatory, consulting and market-access services, with a focus on supporting development of therapies that benefit patients.
The role contributes directly to clinical research technology implementation and the effective collection of digital clinical data.
REQUIRED VERIFIED SKILLS
Bachelor's Degree
Digital Health Technologies
eCOA
eCOA Systems Development
eConsent
Wearables
Sensors
Spirometry
ECG
Clinical Research
Clinical Study Design
UAT
Clinical Data Collection
SOPs
ICH/GCP
Regulatory Guidelines
Trial Management Systems
Microsoft Project Server
Project Management
Vendor Management
Cross-Functional Leadership
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
The supplied posting does not disclose a salary range, bonus structure or specific benefits for this position. Because the role requires a bachelor's degree and 6+ years of relevant industry experience, compensation would generally be assessed at an experienced professional/manager level rather than an entry-level level, but no specific market salary figure should be inferred without verified employer information.
ORGANIZATION CONTEXT & CULTURE
Parexel is a leading global clinical research organization (CRO) that provides comprehensive biopharmaceutical services. They partner with pharmaceutical, biotechnology, and medical device companies to accelerate the development and market access of innovative therapies. Their services span the entire drug development lifecycle, from early-phase clinical research to regulatory consulting and commercialization.
TEAM SIZE: 20,000+ employees
INDUSTRY: Biosciences / Healthcare, Contract Research Organization (CRO)
EXPECTED CAREER ROADMAP
This position provides a strong progression route within Digital Health Technologies, clinical operations and clinical-development technology. Experience managing eCOA and other DHT implementations can lead toward Senior Digital Health Technology Manager, DHT Program Lead, Clinical Technology Lead, Digital Clinical Operations leadership and broader clinical-development technology management roles. The combination of vendor management, UAT, clinical-study implementation, regulatory compliance and cross-functional leadership can also support longer-term opportunities in digital clinical trials, decentralized clinical trials, clinical data strategy and technology consulting.
APPLICATION ADVISORY
Emphasize 6+ years of relevant industry experience and a bachelor's degree. Highlight hands-on experience with eCOA and other Digital Health Technologies such as eConsent, wearables, sensors, spirometry and ECG. Clearly demonstrate clinical-study implementation experience from study design through close-out, including specifications, translations and UAT. Showcase ICH/GCP knowledge, SOP compliance, vendor management, CRO collaboration and project timeline management. Mention experience with trial management systems and Microsoft Project Server if applicable. Prepare examples demonstrating cross-functional leadership, stakeholder training, negotiation, influence, data-driven problem solving and management of multiple deadlines. Quantify the number or complexity of clinical studies, vendors or DHT implementations managed where possible.
RECOMMENDED TRAINING
1/5
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