Clinical Data Analyst Intern 2027

Parexel; Petaling Jaya; Sur place; MYR 20 000 - 29 000; Temps partiel

Résumé du poste

Parexel Malaysia offers a 4- to 6-month internship in Data Management starting January 2027 at Petaling Jaya. This program provides hands-on experience within a multinational environment and exposure to clinically validated data workflows.

You will support data cleaning, CRF reviews, UAT testing, and the preparation of study documents under SOPs and ICH/GCP guidelines. Strong English communication and teamwork are essential; a Bachelor’s degree in a medical field is required.

Qualifications

• Data cleaning and review activities (CDA/Primary CDA)
• Setup of DM documents per SOPs and ICH/GCP
• Lead/perform UAT for clinical databases
• Track and review CRFs and support data entry
• Maintain training compliance and SOP adherence
• Strong problem solving and attention to detail

Responsabilités

• Lead data cleaning and query management
• Support data processing from database setup to lock
• Set up DM documents for Trial Master File
• Perform UAT on database setups and screen reviews
• Track CRFs and assist data entry as needed
• Ensure SOP and ICH/GCP compliance and conduct QC activities
• Maintain training compliance and address training needs

Connaissances

Data cleaning

Query management

SAS listing reviews

UAT testing

CRF review

DM documents

SOP compliance

ICH/GCP knowledge

Team collaboration

English communication

Attention to detail

Time management

Formation

Bachelor’s degree in medical field

Outils

SAS

Description du poste

This is 4 to 6 months internship program starts from January 2027.

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