job description
Join Parexel International, a global leader in clinical research, as a Clinical Data Analyst I in beautiful Bali, Indonesia. This remote role offers the opportunity to contribute to life-changing medical advancements while enjoying a flexible work environment in one of the worldâs most sought-after destinations.
As a Clinical Data Analyst, you will play a pivotal role in ensuring the accuracy and integrity of clinical trial data. You will collaborate with cross-functional teams to clean, review, and validate data, supporting the delivery of high-quality results for our pharmaceutical and biotech clients. This position is ideal for detail-oriented professionals with a passion for data and a commitment to improving global health outcomes.
Parexel offers a dynamic work culture, competitive compensation, and the chance to grow your career in the fast-evolving field of clinical research. Whether you're based in Canggu, Ubud, or any other part of Bali, youâll be part of a global team driving innovation in healthcare.
Responsibility
- Perform data cleaning and data review activities as a Co-Primary or Primary Clinical Data Analyst (CDA).
- Manage and resolve data queries efficiently to ensure dataset accuracy and completeness.
- Generate and review manual/SAS listings to validate clinical trial data.
- Collaborate with data management teams to ensure compliance with study protocols and regulatory standards.
- Assist in the preparation of data specifications and contribute to database design.
- Support the creation of data validation plans and perform quality checks on clinical data.
- Document data issues and work with stakeholders to implement corrective actions.
- Participate in internal and external audits to ensure data integrity and adherence to SOPs.
Qualifications
- Bachelorâs degree in Statistics, Biostatistics, Computer Science, Life Sciences, or a related field.
- 1-3 years of experience in clinical data management, data analysis, or a similar role within the pharmaceutical/biotech industry.
- Proficiency in SAS, SQL, or other data analysis tools; experience with CDISC standards (SDTM, ADaM) is a plus.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Excellent analytical, problem-solving, and communication skills.
- Ability to work independently and collaboratively in a remote setting.
- Attention to detail and a commitment to delivering high-quality, accurate data.
- Fluency in English (written and verbal) is required.