Associate Consultant

Iqvia Biotech

2 - 6 years

8 - 9 Lacs

bengaluru

Posted:16 hours ago| Platform:

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Skills Required

primary research process improvement pharma consulting healthcare life sciences outsourcing analytics secondary research recruitment

Work Mode

Work from Office

Job Type

Full Time

Job Description

Perform extensive research and analysis to build a detailed understanding of the patient experience with a disease and intervention to inform a PRO/COA strategy
- Source information based on robust targeted literature review methods, social media and patient interview transcript analysis
Contribute to project teams in the development and delivery of client deliverables including analysis of IQVIA and public information sources, conducting primary research and independent secondary research
Participating in internal and client meetings and supporting the presentation of project findings to the client
Undertake indication COA landscape assessments to understand key stakeholder demands for patient experience data and how endpoints are being deployed into clinical study designs
- Source information using secondary research methods covering open-source databases and subscription services
Identify and summarise the characteristics of available COA/PRO instruments to measure a specified disease or treatment experience using subscription databases and targeted publication searches
Document and report research in Word and PowerPoint using independent, critical thinking to ensure quality and completeness of output
- Good public domain searching skills to mine information on various pharma topics
Experience in Pharma qualitative analytics, disease landscape assessment, competitive environment, clinical trials analysis, pipeline analysis, treatment algorithms, regulatory environment understanding etc.
Supporting global PCS team to elevate our capabilities, including (but not limited to) the development of intellectual property, marketing materials, training, recruitment and other BD activities

Education & Experience:

Graduate/Post-graduate Degree in Life Sciences from a premier institute (PharmD, MBBS, BDS, Bpharm, Mpharm, Clinical Research etc. )
2-6 years of experience within Pharmaceutical/ Biotechnology/ Consulting/ Professional Services Outsourcing company
Ability to understand clinical trial designs, outcome measures, endpoints, and results
Previous experience with literature reviews and scientific writing is an added advantage
Excellent oral and written communication skills
Must be proficient in Word, Excel, PowerPoint and Internet Explorer
Experience with programmes such as ATLAS. ti or MAXQDA is an advantage

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