Principal Scientist Pharmacometrics

Vizen Life Sciences Pvt Ltd; Hyderabad; On-site; INR 2,500,000 - 4,000,000; Full time

Job summary

Vizen Life Sciences Pvt Ltd in Hyderabad is seeking pharmacometrics specialists to conduct population PK/PD analyses to inform dose regimen decisions and support regulatory submissions. You will write analysis plans, perform analyses, and QC checks while interpreting PK/PD results.

Ph.D. in Pharmaceutical Sciences or related field with 2+ years post-doctoral experience (or MS with 4+ years relevant experience) is required. Strong collaboration in a matrix environment is essential.

Qualifications

• Ph.D. with 2+ years post-doctoral experience or MS with 4+ years of relevant pharmacometrics experience.

Responsibilities

• Write analysis plans and reports, define data requirements and conduct analyses.
• Perform QC checks and interpret PK/PD data and results.
• Model-informed drug development to support regulatory submissions.
• Present findings internally and at external scientific meetings; publish manuscripts.
• Contribute to development of new methodology in pharmacometrics.

Education

Ph.D. in Pharmaceutical Sciences / Pharmacometrics / Chemical/Biomedical/Bio-Engineering or Biological Sciences

Job description

Responsibilities

• Accountabilities with guidance from senior members of the group:
• Conduct population PK, PD, ER analyses to inform?dose regimen selection?and other?key?drug development decisions,?support the design?of clinical?studies and model-informed drug development plans,?and?to support regulatory submissions.
• Write?analysis plans & reports,?define data?requirements,?conduct?analyses, perform quality control (QC) checks,?and interpret PK/PD data and results.?
• Work?effectively in a matrix environment, managing pharmacometrics?deliverables?in accordance with?timelines and overall project goals.?
• Contribute to the development of new methodology and/or applications of pharmacometrics.
• Other Accountabilities & Tasks
• Present?internally and at?external?scientific?meetings; prepare and publish manuscripts in peer reviewed scientific journals; may?participate?in?special interest groups within professional societies.?
• Assist in process improvement initiatives, software validation?and?other technology improvements.
• Carry?out functional responsibilities?in accordance with?applicable SOPs, departmental processes and Regulatory?requirements,?and Johnson & Johnson Credo principles.?

Qualification & Experience

• Ph.D. degree or equivalent in Pharmaceutical Sciences, Pharmacometrics, Chemical/Biomedical/Bio- Engineering or Biological Sciences, with?2+?years of post-doctoral experience or M.S. degree with 4+ years of relevant experience.