CDMA | Clinical Development Medical Affairs

Qualification:
MBBS/BDS/PhD/Master’s in Pharmaceuticals, with relevant post-qualification experience in the scientific and business research space.
Min. Qualification required to man the position: MBBS/BDS/PhD/M.Pharm.

Role Objective:-

• Conducting detailed secondary searches for identification, analysis and reporting of project-relevant data to derive meaningful/actionable insights
• Supporting medical and commercial projects, related to the approval of Global promotional and awareness materials
• Managing Promotional and Non-Promotional content approval process, related to various products within the Business
• Secondary Research into medical journals to verify articles for referencing purpose, to support brand presentations and conferences worldwide

Key Responsibility indicators

People Related:

• Team work - Collaborate with the team, good interpersonal communication, professional conduct, actively participate in team related activities

Process Related:

• Domain Expertise - Demonstrating expertise or quickly gaining knowledge and building expertise in an area of interest
• Efficiency – Effective retrieval of information by identifying relevant data sources, formulating efficient search strategies, critically evaluate information and organize data for analysis
• Accuracy - Ability to assess validity of sources, accuracy of information gathered, data gaps if any and steps to plug in the data gaps
• Quality & Presentation of reports – Good scientific writing with well- structured and formatted content, correct usage of English language, usage of right templates and audience-appropriate representations

Skills 

Must have:

• Clear understanding and exposure to OTC/Consumer/Pharma Healthcare space, demonstrate clear acumen in scientific and business research
• Expertise in secondary research with experience in using databases and open sources.
• Proven strengths/clear aptitude in performing literature analysis and deriving insights
• Report writing skills - creating reports that offer contextually relevant insights
• Knowledge on MS Office (esp. Word, PowerPoint and basic Excel) and Internet searching skills are mandatory
• Good scientific writing with well- structured and formatted content, correct usage of English language.

Must exhibit following core behaviors:

• Taking ownership / accountability of the projects assigned
• Flexibility to work on cross-team projects across all domains
• Attention to details
• Clear/concise and effective communication
• Critical thinking
• Self-motivated, able to work autonomousl

Good to have:

• Should understand the regulatory climate relevant to OTC/Rx space esp. in US/Europe
• Exposure to text mining related projects
• Knowledge of data visualization tools incl. charts and graphs, smart arts etc

Pharma Healthcare, Secondary Research, Scientific writing, OTC, Rx ,OTC Pharma Healtcare,Consumer Pharma Healthcare

Designation: CDMA | Clinical Development Medical Affairs

Vacancies: 5

Experience: 5.0 Year(s) - 7.0 Year(s)