Great opportunity as Senior Clinical Research Associate @ PAREXEL




PAREXEL is a prominent global biopharmaceutical service provider that has been instrumental in assisting the Bio-Tech and Pharmaceutical industries in their efforts to develop new drugs and treatments worldwide. The company offers a diverse range of knowledge-based contract research, medical communications, and consulting services across various therapeutic areas to pharmaceutical, biotechnology, and medical device companies on a global scale. Through its expertise and support, PAREXEL has played a significant role in advancing healthcare and bringing innovative treatments to patients around the world.

Post :Senior Clinical Research Associate

Join Parexel and Make a Significant Impact in Clinical Research

Job Description: At Parexel, the Senior Clinical Research Associate (SCRA) role goes beyond the typical clinical monitor position. As an SCRA, you will play a crucial role in building and maintaining strong site relationships, ensuring their success throughout the clinical trial process. You will serve as the primary point of contact for clinical sites, addressing and resolving any issues or inquiries they may have. Managing site quality and delivery from site identification to close-out will be an essential part of your responsibilities.

Benefits and Opportunities:

  • World-class technology and tailored training based on your expertise
  • Reduced travel and lower protocol load compared to industry peers
  • Bonus incentive program for your hard work
  • Opportunity to work across multiple therapeutic areas
  • Scope for career advancement in clinical research


  • Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites, generating comprehensive visit/contact reports.
  • Foster strong relationships with sites and staff, utilizing problem-solving skills to ensure the integrity of the study.
  • Safeguard the rights and well-being of human subjects, reviewing trial performance at designated sites in accordance with the protocol.
  • Develop patient recruitment strategies in collaboration with clinical sites to meet enrollment timelines and comply with SOPs, protocol/amendments, GCP, and applicable regulatory requirements.
  • Evaluate the quality and integrity of reported data, site efficacy, and drug accountability.
  • Monitor Regulatory Documentation completeness and quality, performing site document verification.


  • Bachelor’s or equivalent degree in biological science, pharmacy, or a related health discipline.
  • Strong understanding of clinical trials methodology and terminology, with experience in clinical research or site management.
  • Ability to work independently and perform all clinical monitoring activities autonomously.
  • Excellent interpersonal, written, and verbal communication skills, working effectively within a matrixed team.
  • Self-driven with a sense of urgency, able to manage multiple tasks and meet project timelines.
  • Ethical work approach to contribute to the development of life-changing treatments for patients.
  • Proficient in computer skills, including knowledge of Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products.

Additional Information:

  • Qualification: B.Pharm, BSc
  • Location: Belgium, Remote
  • Industry Type: Pharma
  • End Date: 30th August 2023

Last Date: 25th August 2023

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