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 high level study feasibility analysis
    • Define analysis plan, derive insights and develop appropriate documents to convey findings from research
    • Conduct clinical and research literature review to support 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 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, 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.
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