Data Scientist - Pharmaceutical/BioTech Firm (5-6 yrs)

Data Scientist

Job Description:

- Accountable for multiple projects/ongoing work activities (timelines, work plans, deliverables) of moderate complexity within a Work Team.

- Accountable for their assigned work supporting the standards/study deliverables and also to assist with the team assignments.

- Review/Develop/Validate/Review datasets, TFL as per CDISC aligned Standards or Data Standards for Study/Project/Portfolio. (Portfolio).

- Contributes to upto 80% of their time to programming deliverables assigned within the scope of the function in either SAS, R or Python and 20% to self-learning, development and growth.

- Explore the existing code base and execute/perform runs as required, also develop/modify as per the needs and specifications suggested to the standards team as appropriate - (Standards Programming).

- Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables across Standards, Programming and Submissions.

- Understand/Implement standard/study/project/portfolio requirements and specification and work with global stakeholders in ensuring completion of project/study/deliverable goals and milestones.

- Knowledgeable in core safety standards as well as TA standards pertinent to their project and lead development of standards necessary for their study.

- Exhibits routine and occasionally complex problem-solving skills, seeking direction when appropriate.

- Regularly update leads on progress and time estimations to ensure smooth daily operations and accurate planning.

- Support in accomplishing department and organization mission by completing assigned tasks.

- Acts as mentor to junior team members.

- Advances job knowledge to next level by participating/contributing in/to opportunities both globally and locally.

- Bachelor or Master (preferred) Degree in Statistics, Computer Sciences, Engineering, Pharmacy, biological sciences, IT, or related field.

- At least 5 - 6 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.

- Understanding of clinical data and drug development process, CDISC standards required.

- Statistical Programming and SAS hand-on experience.

- Clinical trials expertise with an understanding of data operations required for the reporting of clinical.

- Good understanding of ICH and regulatory guidelines.

- Working knowledge of clinical data and relevant data standards.

- Is able to work with stakeholders across time zones under tight timelines.

- Strong written and oral communication skills, and time and project management skills.

- Strong competencies and interests for innovation and problem solving.

- Proven ability to operate with limited oversight.