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Parexel Hiring for Patient Safety Associate I


Apply for Parexel Hiring for Patient Safety Associate I in Hyderabad. Full time position offering drug safety, compliance, and clinical research responsibilities.


Parexel Patient Safety Associate I Recruitment 2025: Full-Time Drug Safety Job in Hyderabad

Parexel, one of the world’s leading clinical research organizations, continues to expand its global operations by strengthening its drug safety and pharmacovigilance teams. The company has announced recruitment for the Patient Safety Associate I position in its Hyderabad location. This is a full-time opportunity for highly motivated graduates and postgraduates aiming to build a long-term career in drug safety, clinical research, and pharmacovigilance operations. Parexel Hiring for Patient Safety Associate I

The position was posted recently, and the last date to apply is November 20, 2025, giving applicants limited time to complete their applications. Candidates who are passionate about improving patient outcomes, supporting clinical trials, and maintaining compliance with global regulatory requirements will find this role an ideal entry point into the world of pharmacovigilance and clinical research. Parexel Hiring for Patient Safety Associate I

In this detailed job post, you will find complete information about the role, including responsibilities, key skills, required educational background, and instructions on how to apply. Parexel Hiring for Patient Safety Associate I


About Parexel

Parexel is globally recognized for its comprehensive clinical development, consulting, and regulatory support services. For decades, the organization has partnered with pharmaceutical companies, biotechnology firms, and medical device manufacturers to develop life-changing therapies. The mission of Parexel is rooted in commitment, empathy, and excellence. Every team member plays a crucial role in bringing new treatments to patients who need them the most. Parexel Hiring for Patient Safety Associate I

Whether the work involves clinical trials, regulatory consulting, or pharmacovigilance operations, Parexel maintains a strong focus on high-quality standards, compliance, and patient safety. Joining Parexel means becoming part of a global network dedicated to improving world health. Parexel Hiring for Patient Safety Associate I

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Role: Patient Safety Associate I

The Patient Safety Associate I plays a significant role in supporting drug safety management activities for both clinical trials and marketed products. The job involves collaborating with medical monitors, safety physicians, and project leaders to ensure that drug safety processes meet international regulatory guidelines and internal standard operating procedures (SOPs). Parexel Hiring for Patient Safety Associate I

The role requires individuals with strong analytical, communication, and documentation skills. As an entry-level position, it provides a structured environment to learn and grow within clinical research and patient safety operations. Parexel Hiring for Patient Safety Associate I


Key Responsibilities

The Patient Safety Associate I is entrusted with a broad range of responsibilities across data processing, reporting, documentation, regulatory submissions, and safety compliance. Below is a detailed description of the key duties: Parexel Hiring for Patient Safety Associate I

1. Drug Safety Case Processing

This position involves hands-on work with Individual Case Safety Reports (ICSRs), an essential part of pharmacovigilance operations. Responsibilities include: Parexel Hiring for Patient Safety Associate I

  • Processing ICSRs received from clinical studies, healthcare providers, literature sources, and other safety channels.
  • Performing triage of incoming safety reports to check for completeness, validity, and legibility.
  • Entering case data into safety databases or tracking systems while ensuring compliance with regulatory timelines.
  • Conducting follow-up requests and managing queries to obtain missing information.
  • Coding case data using standardized medical terminology dictionaries such as MedDRA.
  • Writing clear, accurate, and medically relevant narrative summaries for each case.

These tasks require exceptional attention to detail and adherence to quality standards.

2. Supporting Clinical Trial Safety Activities

The role also involves providing support to clinical trial teams, including:

  • Assisting in the development of project-specific drug safety workflows, procedures, and templates.
  • Supporting safety database configuration and user acceptance testing.
  • Creating and maintaining project files, case documentation, and central project records.
  • Supporting Safety Service Project Leaders (SSPLs) and drug safety specialists during ongoing study operations.
  • Assisting medical monitors and safety physicians as needed.
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3. Regulatory Reporting and Compliance

Compliance with global pharmacovigilance regulations is critical. The Patient Safety Associate I contributes to: Parexel Hiring for Patient Safety Associate I

  • Preparing and submitting expedited safety reports to regulatory authorities, Institutional Ethics Committees (IECs), and investigator sites.
  • Assisting with unblinding of SUSAR (Suspected Unexpected Serious Adverse Reaction) cases when required.
  • Helping with worldwide safety reporting, both electronic and manual submission formats.
  • Tracking submission records, follow-ups, and safety reporting metrics.
  • Ensuring quality control checks for deliverables and identifying reasons for delayed submissions.

4. Literature Search and Signal Management Support

The associate may assist in the literature surveillance process by:

  • Performing literature searches using scientific databases.
  • Reviewing identified articles for potential adverse events.
  • Helping in the early stages of signal detection activities.

5. Audit and Inspection Support

To maintain compliance, the candidate will:

  • Participate in preparation for audits and regulatory inspections.
  • Attend internal and external training sessions related to pharmacovigilance activities.
  • Document procedures and outcomes as per audit requirements.

6. Teamwork and Collaboration

The role involves working closely with cross-functional teams and contributing to collaborative project environments. This includes: Parexel Hiring for Patient Safety Associate I

  • Participating in meetings with clients, investigators, and internal teams.
  • Delegating tasks to Drug Safety Assistants when needed.
  • Informing managers and project leads about potential changes in project scope.

Required Skills

To excel in this role, candidates must possess the following professional skills:

  • Strong analytical and problem-solving skills.
  • Ability to conduct literature and database searches.
  • Excellent verbal and written communication abilities.
  • Good interpersonal skills and professional attitude.
  • Strong organizational and time management skills.
  • Ability to work effectively in a team-oriented environment.
  • Client-focused approach to work.
  • Proficiency in computer applications, including MS Office.
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Educational Qualifications

Applicants must meet one of the following educational criteria:

  • Postgraduate in Pharmacy
  • Postgraduate in Pharmacovigilance and Clinical Research
  • Bachelor in Dentistry (BDS)
  • Life sciences or relevant healthcare background is an advantage

Freshers with strong academic backgrounds in relevant fields are encouraged to apply. Parexel Hiring for Patient Safety Associate I


Experience Required

  • Prior experience in a healthcare or drug safety environment is preferred, but freshers can also apply.
  • Any experience related to medical writing, clinical research, or case processing is an added advantage.

Job Location

  • Hyderabad, India

This is a full-time position within Parexel’s Patient Safety unit.


Why Join Parexel?

Working with Parexel provides a unique opportunity to be part of a global healthcare mission. Key benefits include:

  • Exposure to international drug safety regulations.
  • Extensive training in pharmacovigilance processes.
  • Career growth in clinical research and medical safety operations.
  • Professional development through cross-functional collaboration.
  • A work environment focused on empathy, patient care, and scientific excellence.

How to Apply for Parexel Patient Safety Associate I

Candidates who wish to apply for this position must follow these steps:

  1. Visit the official Parexel careers page.
  2. Search for the job title “Patient Safety Associate I” or use job requisition ID: R0000035109.
  3. Review the job details and ensure you meet the qualification requirements.
  4. Click on the Apply Now button.
  5. Create or log in to your Parexel career profile.
  6. Upload your updated resume and complete the application form.
  7. Submit your application before November 20, 2025.

Ensure your resume highlights relevant coursework, academic achievements, and any experience in drug safety or clinical research. Parexel Hiring for Patient Safety Associate I

For verified pharma job updates, visit PharmaJobHub.in – India’s trusted pharma career portal.

Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.


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