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Clinical Scientific Expert I

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Novartis

13d ago

  • Job
    Full-time
    Junior & Mid Level
  • Research & Development
    Healthcare
  • Hyderabad, +1

AI generated summary

  • You should have experience in clinical research, operations, and project management, with skills in trial protocols, data integrity, and risk monitoring. Cross-cultural collaboration and English fluency are essential.
  • You will implement issue resolution plans, manage program activities, track data, report complaints, distribute samples, review clinical data, and contribute to study documents while embodying Novartis values.

Requirements

  • Work Experience:
  • Cross Cultural Experience.
  • Operations Management and Execution.
  • Collaborating across boundaries.
  • Project Management.
  • Skills:
  • Clinical Research.
  • Clinical Trial Protocol.
  • Clinical Trials.
  • Data Integrity.
  • Learning Design.
  • Lifesciences.
  • Risk Monitoring.
  • Trends Analysis.
  • Languages :
  • English.

Responsibilities

  • Implementing issue resolution plans
  • Assist with program level activities (e.g., tracking of program
  • Managing interactions with relevant line functions including data management, drug supply management, clinical development and/or Novartis Country Pharma Organizations
  • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
  • Distribution of marketing samples (where applicable)
  • Performing clinical data review and insights consistently and accurately which meets the Novartis quality standards, timelines, and is inspection ready
  • High quality contributions to study documents (e.g. protocol, ICF, clinical sections of CTA)
  • Clearly demonstrates Novartis Values and Behaviors (i.e. Innovation, Quality, Collaboration, Performance, Courage and Integrity)

FAQs

What is the primary responsibility of a Clinical Scientific Expert I at Novartis?

The primary responsibility of a Clinical Scientific Expert I is to provide clinical and scientific support throughout all phases of a clinical study, ensuring compliance with Novartis processes, ICH GCP, and regulatory requirements, while delivering study outcomes within schedule and budget.

What are the key performance indicators for this role?

Key performance indicators include the timely execution of assigned trials, effective operational planning with risk mitigation strategies, accurate clinical data review, high-quality contributions to study documents, and demonstrating Novartis values.

What qualifications are required for the Clinical Scientific Expert I position?

The minimum requirements include cross-cultural experience, operations management, project management, and skills in clinical research, trial protocol, data integrity, and risk monitoring.

Where is this position located?

This position is located in Hyderabad, India.

What kind of work experience is preferred for applicants?

Preferred work experience includes operations management and execution, collaboration across boundaries, and project management.

Is knowledge of multiple languages required for this role?

Proficiency in English is required; knowledge of other languages may be beneficial but is not specified as a requirement.

What does Novartis emphasize in its workplace culture?

Novartis emphasizes collaboration, support, and inspiration among employees to achieve breakthroughs that change patients’ lives, as well as building an inclusive and diverse work environment.

Are there any specific compliance standards that a Clinical Scientific Expert I must follow?

Yes, the role requires adherence to Novartis processes, ICH GCP, and other regulatory requirements in all clinical trial activities.

How does the Clinical Scientific Expert I contribute to the clinical trial team?

The Clinical Scientific Expert I is a core member of the Clinical Trial Team and may lead specific aspects of global clinical trials while assisting with program level activities and coordinating with relevant functions.

What kind of accommodations does Novartis provide for individuals with disabilities?

Novartis is committed to providing reasonable accommodations for individuals with disabilities during the recruitment process and employment. Individuals may contact Novartis for assistance if needed.

Science & Healthcare
Industry
10,001+
Employees

Mission & Purpose

Novartis is reimagining medicine to improve and extend people’s lives. As a leading global medicines company, we use innovative science and digital technologies to create transformative treatments in areas of great medical need. In our quest to find new medicines, we consistently rank among the world’s top companies investing in research and development. Novartis products reach nearly 800 million people globally and we are finding innovative ways to expand access to our latest treatments. Around 108,000 people of more than 140 nationalities work at Novartis around the world.

Culture & Values

  • Inspired

    Engage our people. Strive for patients. Live our purpose

  • Curious

    Learn. Be open. Be self-aware

  • Unbossed

    Create clarity. Serve others. Own your actions

  • Integrity

    Be honest. Have courage. Do what’s right