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27/07 Kavita
Head HR at Contify

Views:288 Applications:62 Rec. Actions:Recruiter Actions:39

Contify - Assistant Research Manager - Pharma & Life Sciences (5-8 yrs)

Gurgaon/Gurugram Job Code: 1293518

Program Strategy and Execution:

- Help build strategic plan towards building and growing the Pharma & Life Sciences research team

- Own execution of planned capability building and continuous improvement programs

- Contribute to new business development initiatives

- Drive wins on new pilots/proof of concepts by doing effective solutioning and producing high quality deliverables

Project Management -

- Effectively manage delivery on ongoing projects including ensuring timely and quality delivery

- Ensure timely and effective QC checks on outgoing deliverables

- Recruit and train the right people to become excellent domain analysts

Platform led delivery:

- Read, understand and analyse the content sourced on the Contify platform and publish the content most appropriate to the client use case. Ensure that the Contify's M&CI platform is being optimally leveraged to deliver seamless ongoing intelligence

- Create Market Intelligence newsletters by sourcing articles from the Contify platform and outside (if required)

- Prepare relevant insights and executive summary documents/sections on individual companies; periodically benchmark various companies

- Liaison with the product, engineering, and data team to investigate, report, and resolve platform related issues


- B.Pharm/M.Pharm/B.Tech Biotech graduate with at least 5 years experience in Pharma / Life Sciences market and competitive intelligence research

- At least 4 years' experience in secondary research in pharma / Life Sciences domain with at least three years' project management and solutioning experience

- Experience of working in the US, Europe, and UK markets will be highly preferred

- Primary research experience is not relevant

- Should have strong domain knowledge

- Experience and understanding of "Medical devices/Medtech" domain will be valuable, though not mandatory

- Should have good knowledge about the clinical, commercial, and regulatory processes and frameworks for drug and devices approvals and related events globally

- Should be well versed with publicly available databases like, PubMed, Drugs@FDA, Orange Book as well as paid databases such as Citeline, Evaluate Pharma

- Functional/Technical Skills: Advanced MS PowerPoint and excel skills

- Experience in an Industry/work: 5+ years of experience in business research firms

This job opening was posted long time back. It may not be active. Nor was it removed by the recruiter. Please use your discretion.

Women-friendly workplace:

Maternity and Paternity Benefits

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