PHARMAFull-time
Trainee Clinical Data Analyst
HYDERABAD (IN)REMOTEPOSTED: 9/2/2026
PHARMAFull-time
HIRING ORGANIZATIONPAREXELBiosciences / Healthcare, Contract Research Organization (CRO)
ROLE DEFINITION & RESPONSIBILITIES
Job Overview
Entry-level Trainee Clinical Data Analyst position within Parexel's Clinical Data Management team.
Designed for enthusiastic, detail-oriented graduates beginning their careers in clinical research and clinical data management.
The role supports the collection, review, validation and management of clinical trial data.
Focuses on maintaining clinical data quality and supporting compliance with applicable industry standards and regulatory requirements.
Candidates must be comfortable working in a remote environment.
This is a 6-month contract opportunity.
The company is seeking immediate joiners.
Eligibility is specifically limited to 2025 and 2026 graduates.
Core Responsibilities
Support the collection of clinical trial data.
Assist with reviewing clinical data for completeness, accuracy and quality.
Support validation activities associated with clinical trial data.
Participate in the management and maintenance of clinical research data.
Apply strong attention to detail while reviewing and handling clinical trial information.
Support the Clinical Data Management team in delivering accurate and reliable data for clinical development activities.
Follow established quality standards and applicable processes while performing assigned work.
Contribute to activities that support the integrity and reliability of clinical trial data.
Work collaboratively with team members in a professional clinical research environment.
Develop practical understanding of clinical research and clinical data management processes through on-the-job learning.
Technical & Domain Knowledge
Develop and apply an understanding of clinical trial data collection and management processes.
Build knowledge of clinical data review and validation principles.
Learn and apply ICH-GCP guidelines relevant to clinical research activities.
Develop awareness of applicable local regulatory requirements.
Understand the importance of quality and compliance in clinical trial data handling.
Strengthen logical reasoning and problem-solving abilities for identifying and resolving data-related issues.
Maintain accuracy and consistency while supporting clinical data activities.
Quality & Compliance
Demonstrate strong attention to detail in all assigned activities.
Maintain a commitment to data quality and accuracy.
Support clinical data activities in accordance with applicable industry standards.
Learn and follow ICH-GCP requirements relevant to the role.
Develop knowledge of local regulatory requirements and their relevance to clinical research operations.
Contribute to reliable clinical trial data processes that support the development of therapies intended to benefit patients.
Communication & Team Collaboration
Use strong written English communication skills when performing assigned tasks and interacting with team members.
Demonstrate effective verbal communication skills.
Work collaboratively within the Clinical Data Management team.
Participate effectively in a remote working environment.
Demonstrate a willingness to learn and develop new clinical research and data management skills.
Apply logical reasoning and problem-solving skills when supporting assigned activities.
Candidate Eligibility
Bachelor's degree in Pharmacy, Life Sciences or a related discipline.
Master's degree in Pharmacy, Life Sciences or a related discipline is also eligible.
Only 2025 and 2026 pass-outs are eligible according to the job posting.
Immediate joiners are required.
Candidates should have strong written and verbal English communication skills.
Candidates should demonstrate problem-solving and logical reasoning abilities.
Candidates should have a basic understanding of ICH-GCP guidelines or demonstrate willingness to learn them.
Candidates should have a basic understanding of local regulatory requirements or willingness to learn.
Strong attention to detail and commitment to quality are required.
Candidates must be able to work effectively in a collaborative team environment.
Candidates must be comfortable working remotely.
Contract Details
Contract duration: 6 months.
The opportunity is intended for entry-level graduates who can join immediately.
Company & Career Environment
Parexel operates across clinical development activities including clinical trials, regulatory services, consulting and market access.
The company emphasizes a mission focused on improving global health.
Employees contribute to clinical development activities supporting therapies intended to benefit patients.
The role provides an entry point into professional Clinical Data Management and the broader clinical research industry.
The position offers practical exposure to clinical trial data collection, review, validation, quality and compliance processes.
REQUIRED VERIFIED SKILLS
Clinical Data Management
Clinical Trial Data Collection
Clinical Data Review
Clinical Data Validation
Clinical Data Quality
Attention to Detail
Problem Solving
Logical Reasoning
Written Communication
Verbal Communication
English Communication
Team Collaboration
ICH-GCP Knowledge or Willingness to Learn
Local Regulatory Requirements Knowledge or Willingness to Learn
Remote Working
Pharmacy or Life Sciences Education
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
No salary range, minimum salary, maximum salary or currency is disclosed in the provided official job posting. Compensation for this six-month trainee contract may depend on Parexel's internal compensation structure, employment terms, candidate qualifications and location. Candidates should clarify the monthly or annual compensation, contract benefits, statutory benefits, remote-work support, contract renewal possibilities and opportunities for conversion to longer-term roles during the recruitment process.
ORGANIZATION CONTEXT & CULTURE
Parexel is a leading global clinical research organization (CRO) that provides comprehensive biopharmaceutical services. They partner with pharmaceutical, biotechnology, and medical device companies to accelerate the development and market access of innovative therapies. Their services span the entire drug development lifecycle, from early-phase clinical research to regulatory consulting and commercialization.
TEAM SIZE: 20,000+ employees
INDUSTRY: Biosciences / Healthcare, Contract Research Organization (CRO)
EXPECTED CAREER ROADMAP
This trainee position provides a strong entry point into Clinical Data Management and the wider clinical research industry. During the six-month contract, candidates can build foundational experience in clinical trial data collection, review, validation, quality and compliance. Successful development of these skills can support future opportunities such as Clinical Data Associate, Clinical Data Analyst, Clinical Data Coordinator and more advanced Clinical Data Management roles. With additional experience, professionals may progress toward senior data management, database management, data quality, clinical operations, data standards or project leadership positions. Knowledge of ICH-GCP and regulatory requirements can also create opportunities across CROs, pharmaceutical companies and clinical research organizations.
APPLICATION ADVISORY
Highlight your 2025 or 2026 graduation year clearly at the top of your resume and mention your immediate availability. Emphasize your Bachelor's or Master's qualification in Pharmacy, Life Sciences or a related discipline. Include academic projects, internships, coursework or practical exposure related to clinical research, clinical trials, data management, data analysis, quality or regulatory requirements. Demonstrate attention to detail through specific examples of reviewing data, identifying errors or maintaining accuracy. Prepare to discuss basic ICH-GCP concepts, the importance of clinical data quality and why accurate clinical trial data is essential for patient safety and research outcomes. Showcase logical reasoning, problem-solving and English communication skills. For interviews, be prepared to explain why you want to build a career in Clinical Data Management and confirm your comfort with remote work and a six-month contract.
RECOMMENDED TRAINING
1/5
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