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Parexel

Clinical Data Analyst Intern 2027

Parexel Petaling Jaya, Selangor, Malaysia

Pharmaceutical Manufacturing · 10,001+ employees

Oct 19
data-analyst Junior (0-2 yrs) Internship Malaysia
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About the role

The intern will be responsible for data cleaning, query management, and supporting database setup and reconciliation activities. They will also perform user acceptance testing and ensure compliance with standard operating procedures and ICH/GCP guidelines.

What they look for

Data validation Data cleaning Query management SAS listing reviews Database setup Data reconciliation Trial master file User acceptance testing Clinical database CRF tracking Problem-solving Logical reasoning Attention to detail Time management Communication skills Technical learning

Requirements

Candidates must hold a bachelor's degree or relevant medical qualifications and demonstrate strong logical reasoning and attention to detail. Proficiency in English and the ability to work collaboratively in a team environment are required.

Full 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 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

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