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Parexel Hiring for Multiple Positions in India: Study Start-Up Leader, Clinical Research Associate , and Document Specialist

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Parexel, a leading global clinical research organization (CRO), is currently hiring for multiple positions in India, including Study Start-Up LeaderClinical Research Associate II (CRA II), and Document Specialist I. These roles are based in Bengaluru and offer remote opportunities for eligible candidates. If you are passionate about improving global health and have a background in clinical research, regulatory affairs, or project management, this is your chance to join a company that values innovation, collaboration, and patient-centric solutions.

Why Parexel?

At Parexel, our mission is to improve the world’s health. From clinical trials to regulatory consulting and market access, every solution we provide is driven by a deep conviction to make a difference. Each team member, regardless of their role, contributes to the development of therapies that ultimately benefit patients. We take our work personally, approach it with empathy, and are committed to delivering high-quality results.

Open Positions at Parexel India

1. Study Start-Up Leader

Location: Bengaluru, India
Job ID: R0000031329

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Key Responsibilities:

  • Manage the study start-up process, including site activation strategy, regulatory submissions, and document collection/approval.
  • Coordinate critical path planning for site initiation, EC/RA submissions, and ICF customization.
  • Collaborate with global study teams to ensure timely delivery of study start-up activities.
  • Proactively identify risks and develop mitigation strategies to meet project timelines.
  • Maintain up-to-date systems for tracking study start-up progress and metrics.

Skills Required:

  • Knowledge of ICH-GCP guidelines and international regulatory requirements.
  • Strong leadership, problem-solving, and conflict management skills.
  • Excellent communication and client-facing abilities.
  • Ability to work in a matrix environment and lead virtual teams.

Qualifications:

  • Degree in life sciences or related field.
  • Proven experience in study start-up activities within a CRO or pharmaceutical company.

2. Clinical Research Associate II (CRA II)

Location: Bengaluru, India
Job ID: R0000031331

Key Responsibilities:

  • Act as the primary point of contact for assigned sites during the start-up and maintenance phases.
  • Conduct site qualification visits, negotiate contracts, and manage regulatory submissions.
  • Ensure compliance with study protocols, ICH-GCP guidelines, and local regulations.
  • Monitor site performance, data quality, and patient recruitment strategies.
  • Prepare and submit essential documents to the Trial Master File (TMF).

Skills Required:

  • Strong site management and clinical trial monitoring experience.
  • Excellent organizational, communication, and problem-solving skills.
  • Proficiency in Clinical Trial Management Systems (CTMS) and MS Office.
  • Ability to travel as required.

Qualifications:

  • Degree in biological sciences, pharmacy, or a related field.
  • Minimum of 2-3 years of experience as a CRA or equivalent role.

3. Document Specialist I

Location: Remote (Bengaluru/Mumbai)
Job ID: R0000031065

Key Responsibilities:

  • Compile and publish clinical study report appendices in compliance with regulatory requirements.
  • Format clinical documents using MS Word and ensure submission-ready deliverables.
  • Manage document distribution and maintain project files.
  • Provide quality control reviews for draft and final documents.
  • Support project teams with document-related issues and training.

Skills Required:

  • Knowledge of global regulatory submission formats and publishing best practices.
  • Proficiency in MS Office and document management systems.
  • Strong attention to detail and organizational skills.
  • Ability to work independently and meet tight deadlines.

Qualifications:

  • Degree in life sciences or related field.
  • Prior experience in document compilation or regulatory submissions preferred.

Why Join Parexel?

  • Impactful Work: Contribute to the development of life-saving therapies.
  • Global Exposure: Work with a diverse, international team.
  • Career Growth: Access to training, mentorship, and advancement opportunities.
  • Work-Life Balance: Flexible work arrangements and remote opportunities.

How to Apply

If you are ready to take the next step in your career, apply for these exciting opportunities at Parexel. Visit the Parexel careers page and search for the respective job IDs:

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