Clinical Data Analyst Intern at Parexel
, , Malaysia -
Full Time


Start Date

Immediate

Expiry Date

13 Feb, 26

Salary

0.0

Posted On

15 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Problem-Solving Skills, Logical Reasoning, Attention To Detail, Time Management, Prioritization Skills, Team Collaboration, Interpersonal Skills, Oral Communication, Written Communication, Learning Ability, Knowledge Sharing, Flexibility, Accountability

Industry

Pharmaceutical Manufacturing

Description
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. This is 6 months internship program starts from January 2026. Location: Petaling Jaya, Parexel Malaysia Office Key Accountabilities: Data Validation (cleaning) Responsible for/start to lead data cleaning and data review activities (Co-Primary CDA/Primary CDA), e.g. query management and manual/SAS listing reviews. Support/start to lead data processing activities from database setup to database lock, e.g. external vendor data reconciliation. Data Management Documents/Plans (Trial Master File) Perform and/or support the setup of DM documents and ensure proper documentation as per Standard Operating Procedures, ICH/GCP Guidelines. Study Start-Up Activities and User Acceptance Testing (UAT) Start to lead/perform user acceptance testing on clinical database setups. Start to review protocols and EDC Entry Screens if required. Data Tracking and Entry Track and review CRFs. Support data entry where required. Project Quality Management & Compliance Training Ensure compliance to Standard Operating Procedures, ICH/GCP Guidelines. Support/start to lead functional QC activities on databases and/or patient data, as per business needs. Maintain training compliance as per Job Roles assigned, including On-the-Job training. Address training needs, as per Development Goal/s identified. Skills: Evidence of strong problem-solving skills and logical reasoning Commitment to first time quality, including a methodical, analytical and accurate approach to work activities (attention to detail) Time management and prioritization skills in order to meet objectives and timelines Evidence of ability to work collaboratively within a team environment Good interpersonal, oral and written communication skills Learning ability and knowledge sharing approach; swift understanding of technologies and new processes A flexible attitude with respect to work assignments and new learning; ability to adjust rapidly to changing technical environments Evidence of accountability relative to Key Accountabilities in Job Description Written and oral fluency in English Education: Bachelor’s degree and/or other medical qualifications. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.
Responsibilities
The Clinical Data Analyst Intern will be responsible for data validation, cleaning, and review activities, as well as supporting data processing from database setup to lock. They will also assist in user acceptance testing and ensure compliance with standard operating procedures and guidelines.
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