Parexel CDM jobs as Senior Clinical Data Analyst – Lifescience candidates
Welcome to Parexel’s Job Posting for Senior Clinical Data Analyst:
Parexel is a leading global biopharmaceutical services company that focuses on improving client success through innovative and quality solutions. We are dedicated to bringing life-changing therapies to patients worldwide.
Job Details:
- Position: Senior Clinical Data Analyst
- Location: India, Remote
- Additional Locations: India-Bengaluru; India-Bengaluru-Remote; India-Mumbai-Remote
- Job ID: R0000031254
- Category: Data Management
About this Role:
The Senior Clinical Data Analyst (SCDA) will play a vital role in performing and leading clinical data validation activities, providing technical expertise, and ensuring operational excellence in Data Management processes and documents. The SCDA will serve as a subject matter expert on DM Systems/processes, offering support to both internal and external stakeholders.
Roles and Responsibilities:
- Proven leadership in global, cross-functional team settings; skilled in task coordination and prioritization in the Primary CDA role.
- Strong stakeholder management: independently engages with sponsors on data issues and validation needs.
- Excellent negotiation, influence, and problem-solving skills; adept at decision-making in ambiguous situations and root cause analysis.
- High commitment to quality and detail; methodical and analytical approach.
- Effective time management with urgency to meet objectives.
- Strong interpersonal, written, and verbal communication; diplomatic and audience-appropriate.
- Confident presenter and quick learner with a collaborative, knowledge-sharing mindset.
- Adaptable to changing environments with a proactive learning attitude.
- Strong sense of accountability and drive for continuous improvement in DM efficiency.
- Fluent in English; in-depth understanding of DM processes, data validation, and regulatory guidelines (ICH-GCP, local regs, SOPs).
- Proficient in CDMS (e.g., InForm, Rave, Veeva, etc.); knowledge of SAS, CDISC, and medical coding dictionaries (MedDRA, WHODRUG).
- Well-versed in study lifecycle DM activities, including database setup and validation.
- Awareness of project financials, budget forecasting, and scope management.
- Experience in the clinical research industry and team collaboration on DML-level activities.
For detailed requirements and qualifications, please refer to the original notification.
