* Salary estimates based on industry data for similar roles
Launch Your Career Ensuring Data Integrity in Global Clinical Trials
At PAREXEL, we are a leading clinical research organization (CRO) where the integrity of clinical data is paramount. Every data point we manage represents a patient's contribution to scientific discovery, and the accuracy of our work directly impacts the development of new treatments.
We are seeking a detail-oriented and proactive Clinical Data Associate to join our dynamic team. This is a foundational role where you will be trained to become an expert in data management processes, from study start-up through to database lock. You will play a hands-on role in cleaning, validating, and managing clinical trial data, ensuring it meets the highest standards of quality and regulatory compliance (ICH-GCP). This is an excellent opportunity to build a rewarding career at the operational core of global drug development.
Your Mission: Become an Expert in Clinical Data Integrity
You will be responsible for the crucial tasks that transform raw clinical data into reliable, analysis-ready datasets, forming the evidence base for regulatory submissions.
Key Responsibilities:
- Data Cleaning & Validation: Take ownership of data cleaning activities, including query management and meticulous review of data listings, to identify and resolve discrepancies. Progress from supporting to leading these activities as you gain experience.
- Study Start-Up & Database Testing: Contribute to study start-up by performing User Acceptance Testing (UAT) on clinical databases to ensure they are set up correctly for data collection.
- Data Management Documentation: Support the setup and maintenance of essential Data Management documents, ensuring all work is accurately documented in the Trial Master File (TMF) in compliance with SOPs.
- Process Execution & Quality Control: Execute data management tasks according to established timelines, supporting functional quality control (QC) checks to ensure the highest standard of first-time quality.
- Continuous Learning: Maintain training compliance and proactively develop your skills in clinical data management systems, medical terminology, and regulatory guidelines.
About You: The Ideal Candidate
You are a meticulous, analytical problem-solver with a passion for quality and a desire to learn the intricacies of clinical research.
Required Qualifications & Mindset:
- A Bachelor’s degree in a life science, nursing, or related field, or equivalent relevant industry experience.
- A basic understanding of the clinical research industry and data management processes.
- Excellent attention to detail and a commitment to accuracy in all tasks.
- Strong problem-solving skills and a logical, analytical approach to work.
- Excellent time management and the ability to prioritize tasks to meet deadlines.
- A collaborative spirit with strong interpersonal and communication skills in English.
- A flexible, proactive attitude and a swift ability to learn new technologies and processes.
Technical Exposure (You will be trained on these):
- Basic awareness of Clinical Data Management Systems (e.g., InForm, Rave, Veeva).
- Basic knowledge of medical terminology and coding dictionaries (e.g., MedDRA, WHODRUG).
- Understanding of ICH-GCP guidelines and data validation flows.
Why This Role is a Career Launchpad:
- Build a High-Demand Skill Set: Receive comprehensive training in clinical data management, a critical and specialized function within the booming life sciences industry.
- Clear Growth Path: The role is structured for growth, with a clear trajectory from supporting to leading key data management activities (e.g., from Co-Primary to Primary CDA).
- Meaningful Impact: See the direct results of your work in the data that supports the development of new medicines and therapies for patients.
- Global Environment: Join a world-leading CRO and collaborate with a diverse, international team.
- If you are a sharp, quality-focused individual looking to start or advance your career in clinical research, we encourage you to apply.
