Job Description

Experience levels: 2+ years
Location: Ahmedabad Requirements: We are looking for a consultant to work with our clients on topics including real-world evidence, clinical research, and epidemiology. Candidates will work closely with our clients on the following topics:

• • Design RWE studies for clinical research across different disease areas.
  • Identify the right datasets for different studies based on the use case, intended variables and outcomes, and available data sources.
  • Conduct a high-level study feasibility analysis.
  • Define an analysis plan, derive insights, and develop appropriate documents to convey findings from the research.
  • Conduct clinical and research literature reviews to support the above activities.

The ideal candidate for this role should have 2+ years’ experience conducting research in the pharma industry, contract research organization, or academic institute; or experience in a closely related discipline within the pharma industry. The candidate should have experience in at least a few of the below-listed activities:

• • Experience in setting up, coordinating, and supervising clinical studies
  • Knowledge of randomized controlled clinical trials principles, methodology, and procedures.
  • Independently draft and edit documents such as high-level research proposals and protocols.
  • Knowledge of the pharmaceutical industry, terminology, and practices.
  • Knowledge of RWE data sources and standards such as MarketScan, CPRD, JMDC, Optum, PharMetrics, and OMOP.
  • Developing strong working knowledge in diseases and therapeutic areas.
  • Strong research and data collection skills.

The candidate should also have the below-mentioned project management and communication skills:

• • Support project management by coordinating project activities and timelines as well as issue management.
  • Liaise with internal and external stakeholders to provide a single point of accountability for workflow management through the organization, across multiple internal and external work streams.
  • Ability to liaise with doctors, consultants, or investigators to facilitate study execution.
  • Summarize meetings, document scopes of work & project charters, provide status updates, and create reports and presentations for internal and external audiences.
  • Identify resource/schedule bottlenecks and work with internal teams to mitigate risks or escalate as appropriate.
  • Proficient with Microsoft Office Word, Excel, and PowerPoint.
  • Ability to develop and deliver both oral and written presentations.