Senior Data Integration Analyst

Manpowergroup Services India; Hyderabad; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

ManpowerGroup Services India is seeking a Senior Data Integration Analyst for our Hyderabad Hub. You will lead the integration of clinical trial data, implementing data flows and mapping to meet our clinical data hub standards while ensuring GCP compliance and timely delivery.

Collaborating with Clinical Data Managers, study teams and external providers, you will coordinate specifications, testing and data transfers across CDISC standards, eSource and related technologies, helping to maintain

Qualifications

• 3+ years in clinical data management with 1+ year in external data integration/mapping.
• Strong knowledge of CDISC/CDM standards and regulatory guidelines (ICH E6/E8).
• Experience coordinating data integration activities with internal/external stakeholders.
• Proven ability to map data flows to clinical data hub standards and ensure data quality.

Responsibilities

• Deliver high-quality CDM data integration deliverables and data mapping specifications.
• Coordinate data flow implementation with external providers and internal teams.
• Collaborate with Clinical Data Manager, Study Manager, Statistician and Quality teams.
• Identify data integration issues and drive timely resolution and continuous improvement.
• Analyze new requirements and propose technical solutions; support new analysts.

Skills

Collaboration & communication

CDM knowledge (ICH E6/E8)

Data integration & mapping

GCP compliance

CDISC standards

SAS / R / Python basics

Problem solving & critical thinking

Education

Bachelor’s or Master of Science in life science or related field

Tools

SAS

R

Python

AI automation tools

Job description

Job title: Senior Data Integration Analyst

• Location: Hyderabad, India
• Grade: L2-1

About the job

Our Hubs are a crucial part of how we innovate, improving performance across every our department and providing a springboard for the amazing work we do. Join our Hyderabad Hub, build a career and you can be part of transforming our business while helping to change millions of lives.

Ready? As Senior Data Integration Analyst within our Hyderabad Hub, you will play a key role in the integration of data collected through clinical trials, contributing significantly to implementing tools to enhance data flow management.

Your responsibilities will include the implementation of data flows and data mapping to meet the organization's clinical data hub standards and ensuring compliance with GCP and applicable regulatory guidelines. You will ensure that all activities are completed according to agreed-upon standards and timelines, while also providing support to guarantee the accuracy and reliability of the data.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve peoples lives. Were also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main responsibilities:

• Accountability for the quality of CDM data integration deliverables (such as FTS (File Transfer Specification), DTA (Data Transfer Agreement), Data Mapping specification and implementation) and for the delivery of accurate and reliable clinical study data.
• Coordinating study data integration activities for the data flow implementation with external providers and internal stakeholders: specifications, implementation, testing including data collected through Central Labs, eCOA, IRT, connected devices, telemedicine, HR, and mobile healthcare.
• Liaising directly with internal customers (Clinical Data Manager, Global Study Manager, Study Medical Manager, Statistician, Quality, etc.) and external providers to coordinate all clinical data integration activities for studies and discussing timelines.
• Proactively anticipating and addressing data integration issues arising during study conduct and monitoring them until resolution.
• Identifying areas for continuous improvement and actively participating.
• Analysing new requirements from customers and proposing technical solution strategies.
• Providing support in the implementation of specific data flows and offering assistance to new Data Integration Analysts.

About you

Experience:

• At least 3 years experience in clinical data management and more than 1 years in external data integration and mapping.

Soft and technical skills:

• Good collaboration and communication skill
• Strong experience with CDM and related regulations (incl. ICH E6 and E8).
• Solid risk-based mindset focusing on Quality by Design (QbD) and on what really matters.
• Learn and adapt quickly when facing new problems. Think critically and use rigorous, objective, and pragmatic methods to solve multidimensional problems with effective and timely solutions.
• Experienced in CDISC standards /terminologies in Clinical Data Standards
• Good knowledge in data transfer and data mapping using digital tools.
• Anticipate delivery risks, bottlenecks, issues, and delays to proactively prevent themor minimize their impact.
• Understanding of advanced drug development concepts such as Decentralized Clinical Trials (DCT), Master & Adaptive Protocols, eSource. Programming languages (SAS, R or Python) and AI Based automations is a plus.

Education:

• Bachelor or Master of Science degree or above, preferably in a life science or mathematics-related area (e.g., Pharmaceutical, medical, or mathematics, computer science or similar technical fields).

Languages:

• Strong English skills (verbal and written), ability to exchange fluently in a global environment.

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
• Join an international innovative biopharma company.
• Lead a clinical data technology team working on several therapeutic areas.
• Participate in the evolution of Clinical Data Management and deployment of innovations