Associate Digital Health Technologies Manager

Parexel; Hyderabad; On-site; INR 1,800,000 - 3,200,000; Full time

Job summary

Parexel in Hyderabad, India seeks a Digital Health Technology Associate Manager to drive the implementation of digital health tools (eCOA, econsent, wearables) from study design to closeout. You will manage timelines, coordinate UAT, and ensure SOP/ICH-GCP compliance while leading cross-functional teams and vendor partners.

You will also train stakeholders, translate specifications into actionable plans, and maintain adherence to regulatory guidelines and data governance across internal and

Qualifications

• Bachelor's degree in a relevant field and minimum 6+ years of experience in clinical research or digital health.
• Knowledge of digital tools and technologies used in clinical trials, eCOA and eConsent processes.
• Strong interpersonal, leadership and vendor management skills.
• Ability to plan, execute and solve problems with a data-driven approach.
• Excellent written and verbal communication; capable of influencing/stakeholder management.

Responsibilities

• Manage project timelines and oversee UAT activities for digital health tools.
• Coordinate with clients and CROs, ensure SOP/ICH-GCP compliance.
• Oversee vendor activities and provide training to stakeholders.
• Translate specifications into actionable project plans and deliverables.

Skills

Project management

Vendor management

Cross-functional leadership

UAT execution

Communication

Strategic planning

Time management

Negotiation

Industry trends

Clinical trial systems

Education

Bachelor's degree

Tools

eCOA systems

Trial management systems

Microsoft Project Server

Data governance

Job description

The Digital Health Technology Associate Manager (DHT AM) is responsible for the implementation of digital tools and technologies (e.g. electronic COA (eCOA), econsent, wearables, sensors, spirometry, ECG, etc.) in individual clinical research studies from study design to close out in collaboration with the study team. In this role, a typical day may include: Managing project timelines, translation, specifications, UAT activities, including either direct participation in UAT execution or oversight of UAT activities, and ensuring collection of such data is in accordance with Client Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs). Responsible for managing vendor activities, and training & education of stakeholders.

Job Requirements

• Demonstrate knowledge of some digital tools and technologies. Specifically, eCOA systems development processes
• Demonstrated interpersonal & leadership skills
• Ability to understand the strategic direction and guidance for respective clinical studies
• A data driven approach to planning, executing, and problem solving
• Effective communication skills via verbal, written and presentation abilities
• Ability to independently perform and manage multiple tasks at one time and meet deadlines in a complex environment working both internal to Client and external vendors
• Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization
• Ability to influence and negotiate
• An awareness of relevant industry trends
• Demonstrated vendor management experience
• Technical knowledge of trial management systems and Microsoft Project Server
• Knowledge of ICH/GCP and regulatory guidelines/directives
• Effective project management skills, cross-functional team leadership and organizational skills

Minimum Years Of Experience

Bachelor's degree and minimum of 6+ years of relevant industry experience.