Genpact is looking for a Clinical Data Management Lead & Training Specialist to take charge of high-quality clinical data delivery and capability development within our growing healthcare division.

Key Responsibilities
1. Lead end-to-end Clinical Data Management (CDM) activities across global studies.
2. Ensure data accuracy, integrity, and compliance with GCP, ICH, and regulatory guidelines.
3. Oversee database setup, data validation, discrepancy management, and quality checks.
4. Mentor junior team members and foster a strong learning culture.

Required Skills & Qualifications
Bachelors or Masters degree in Life Sciences / Pharmacy / Biotechnology.
610+ years of strong experience in Clinical Data Management.

Drive Innovation in Clinical Research with Cadila Healthcare Ltd.!
Join our growing Clinical Operations team and contribute to high-quality clinical trials that impact patient health globally. We are seeking a Senior Clinical Research Associate (Sr. CRA) with strong expertise in monitoring, site management, and regulatory compliance.

Qualifications:
1. Bachelors or Masters degree in Life Sciences, Pharmacy, Nursing, or related field
2. Minimum 36 years of CRA experience, ideally in pharma or CRO
3. Strong working knowledge of ICH-GCP & clinical trial regulations
4. Excellent communication, analytical, and documentation skills
5. Ability to manage multiple study sites independently.

Desired Skills:

1. Expertise in monitoring oncology, metabolic, or specialty therapeutic areas
2. Proficiency with EDC platforms (Medidata, Oracle, Veeva, etc.)
3. Strong interpersonal and site management capabilities
4. Problem-solving mindset with attention to detail

We are seeking a highly skilled Clinical Data Management (CDM) Lead & Training Specialist to oversee end-to-end data management activities and drive training initiatives across clinical projects. The ideal candidate should have strong leadership, technical expertise, and a passion for developing teams in a clinical research environment.

Key Responsibilities
Clinical Data Management Leadership

Lead and manage clinical data management activities across multiple studies.

Oversee database design, CRF development, data validation, edit checks, and query management.

Ensure data quality, accuracy, and compliance with industry standards (ICH-GCP, CDISC, FDA, EMA).

Collaborate with cross-functional teams including Biostatistics, Clinical Operations, Programming, and QA.

Conduct risk evaluations and implement data-cleaning strategies to ensure high-quality deliverables.

Ensure timely database lock and submission-ready datasets.

Review and approve study documents: DMPs, DVGs, CRFs, annotation, and specifications.

Training & Development

Design and deliver training programs for CDM teams covering tools, processes, SOPs, and best practices.

Conduct onboarding and continuous capability-building sessions for new and existing team members.

Evaluate training effectiveness and implement improvements.

Develop competency frameworks, assessments, and skill-development roadmaps.

Document training activities and maintain compliance with regulatory requirements.

Be part of a mission-driven organization committed to advancing global clinical research while ensuring patient safety at every step.

Position Overview

As a Pharmacovigilance / Drug Safety Associate, you will handle essential drug safety operations, ensuring accuracy, compliance, and timely reporting of safety data for global studies.

Key Responsibilities

Process and review Individual Case Safety Reports (ICSRs)

Ensure compliance with global pharmacovigilance regulations and SOPs

Conduct quality checks and case evaluations

Support signal detection and safety risk management

Maintain safety databases and documentation

Assist with periodic safety reports (PSURs, DSURs, PADERs)

Coordinate with internal teams for timely submissions

Qualifications

Bachelors/Masters in Pharmacy, Life Sciences, Biotechnology, or Nursing

13 years of experience in Pharmacovigilance or Drug Safety

Experience with safety databases (Argus, ArisG, etc.)

Knowledge of global PV guidelines (ICH, EMA, FDA)

Strong communication, attention to detail, and analytical skills.

Pfizer is seeking a skilled Automation Java Developer to join our global digital technology team. In this role, you will design, develop, and maintain automation frameworks and tools that enhance our software delivery process. Youll collaborate with cross-functional teams to ensure reliability, scalability, and performance of automation solutions supporting critical healthcare and pharmaceutical platforms.

Key Responsibilities:

Design, develop, and maintain Java-based automation frameworks for backend and API testing.

Implement automated testing strategies for web, API, and microservices applications.

Collaborate with QA, DevOps, and development teams to integrate automation into CI/CD pipelines.

Troubleshoot and optimize test execution to ensure efficient continuous testing.

Develop reusable components and utilities to support test automation efforts.

Document automation processes and maintain clear, reusable scripts.

Participate in Agile ceremonies (daily stand-ups, sprint planning, retrospectives).

Required Skills & Qualifications:

Bachelors degree in Computer Science, Engineering, or related field.

36 years of experience in Java development and test automation.

Hands-on experience with Selenium, TestNG, RestAssured, or Cucumber.

Strong understanding of API automation, CI/CD tools (Jenkins, Git, Maven), and version control.

Knowledge of cloud-based testing environments (AWS, Azure) is an advantage.

Excellent problem-solving and analytical skills.

Strong communication and collaboration abilities in a global team setup.

Key Responsibilities:

Design, develop, and maintain scalable Java-based applications.

Write clean, efficient, and well-documented code.

Collaborate with cross-functional teams including QA, DevOps, and Product.

Participate in code reviews, unit testing, and debugging.

Implement new features and optimize existing systems for better performance.

Stay updated with emerging technologies and development best practices.

Required Skills & Experience:

Bachelors degree in Computer Science, Engineering, or related field.

26 years of hands-on experience in Java development.

Strong knowledge of Spring / Spring Boot, RESTful APIs, and Microservices architecture.

Experience with SQL / NoSQL databases (MySQL, MongoDB, etc.).

Familiarity with version control systems (Git, GitHub, Bitbucket).

Understanding of Agile methodologies and CI/CD pipelines.

Excellent problem-solving and analytical skills.

Preferred Skills:

Experience with cloud platforms (AWS, Azure, or GCP).

Knowledge of Docker, Kubernetes, or other containerization tools.

Familiarity with front-end technologies (Angular, React) is a plus.

Were looking for an experienced SAP Hybris professional with strong knowledge in eCommerce platform development, integration, and customization. Youll collaborate with cross-functional teams to deliver scalable digital commerce solutions.

Were looking for an experienced SAP Hybris professional with strong knowledge in eCommerce platform development, integration, and customization. Youll collaborate with cross-functional teams to deliver scalable digital commerce solutions.

Role Overview

Provide operational support to Clinical Supply Chain Study Leaders for multiple studies across all phases (set-up, follow-up, closure).
Work independently and collaborate with multiple leaders and cross-functional teams.
Preparing and tracking transfer orders.
Managing stock reconciliation.
Performing quality checks.
Preparing documentation for labeling and shipments.
Monitoring needs for destruction.
Archiving documents in the electronic Trial Master File.
Key Responsibilities

Support clinical supply chain operations for global studies.
Ensure compliance with regulatory standards and protocols.
Maintain accurate documentation and inspection readiness.
Communicate effectively with supply chain leaders, operational teams, and outsourcing partners.
Adapt to changing priorities in a fast-paced environment.
Must-Have Skills & Qualifications

Education: Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD).
Clinical supply support or logistics for clinical trials (Phase I-IV).
Digital tools and supply chain software.
Regulatory standards (quality, safety, documentation).
Investigational product management (kit types, shelf life, depot management, distribution, reconciliation, returns, destruction).
Proficiency with tools: IRT (e.g., Endpoint, Suvoda), Smart Supplies, Veeva Vault.
Documentation and quality check skills.
Fluent English for communication with stakeholders.
Key Competencies

Attention to detail and organizational skills.
Ability to manage multiple priorities and work collaboratively in a multicultural environment.
Strong problem-solving and adaptability skills.
Comfort with digital tools and documentation processes.

Your responsibilities include, but are not limited to:
May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of clinical protocols, amendments and related documents; drive and/or supprt trial-related documents and processes.
development of clinical section of regulatory documents like Investigators Brochure, safety updates, IND/NDA submission documents, responses to Health Authorities questions.
support the global multidisciplinary CTT to ensure all trial results are met according to timelines, budget, quality standards and operational procedures: attend CTT meetings, assist in report study progress and issues.
support the CTL/Lead CTL, in the ongoing review and cleaning of the clinical trial data, support final analysis and interpretation including the development of clinical trial reports, publications and internal/external presentations.
coordinate the real time availability of quality clinical trial data, including safety, efficacy, pharmacokinetic, imaging and biomarker data, to provide consolidated information for dose escalation meetings with investigators.
Responsible for accuracy of trial information in all trial databases and tracking systems. Attend relevant meetings to support ongoing execution of clinical trial and program level activities.
ensure that program specific standards/activities (e.g., CRFs, UAT testing, database specifications, Data Handling plan, outsourcing specifications including imaging, biomarkers, PK, data monitoring, validation plans and data transfer specifications) are applied to the clinical trial, where applicable.
develop clinical outsourcing specifications to facilitate bid templates and selection of CROs and other 3rd parties including central lab and imaging vendors; handle work with external vendors in collaboration with the CRO; Management Department as well as with the Assay Research Lab. This also includes the set-up, logistics, documentation and clinical supplies needed for the clinical trial(s).