DDReg Pharma Pvt. Ltd.

DDReg Pharma is a global life sciences consulting firm specializing in regulatory affairs, pharmacovigilance, and quality services. With over 15 years of experience, they help pharmaceutical,…

Drug SafetyGMP ComplianceIPRLife SciencesPharmacovigilanceRegTechRegulatory AffairsRegulatory Intelligenceddregpharma.com

DDReg Pharma Pvt. Ltd.

DDReg Pharma is a global life sciences consulting firm specializing in regulatory affairs, pharmacovigilance, and quality services. With over 15 years of experience, they help pharmaceutical,…

Drug SafetyGMP ComplianceIPRLife SciencesPharmacovigilanceRegTechRegulatory AffairsRegulatory Intelligenceddregpharma.com

HQGurgaon, IN

Team Size88

Open Jobs4

Total Funding-

Latest FundraiseUnknown

Join the Team

Medico Marketing _Onsite (GGN)_ 3+ yrs

On-SiteGurgaon, Haryana, IN

On-Site • Gurgaon, Haryana, IN

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Job Descriptions

Lead creation and review of scientific content: disease education decks, MOA visuals, scientific FAQs, white papers, leave‑behinds, patient education, and omnichannel copy.
Maintain message maps and claims repositories with references and tiered levels of evidence.
Ensure consistency across channels (digital, field, conferences, PR) and alignment with labeling and regulatory guidance.
Writing the scientific content to be published in website, Validate the scientific claims made in any promotional material or reference checking, Interacting with KOL for promotional campaign and preparing slide deck for CME, Develop content/script for promotional video
Translate complex scientific/regulatory information into client-friendly marketing communication.
Support development of white papers, scientific content, webinars, and thought leadership materials.
Support with Medical content for KOL/HCP engagement & scientific exchanges (non‑promotional, compliant). Capture insight summaries (medical needs, barriers, sentiment) to inform evidence generation and messaging.
Peer review and literature search to analyse & integrate the information to be understood by KOLs and different medical fraternity.
Development of product monograph; Search medical database to identify literature articles supporting the product/process. Review of product safety profile. Carry out risk-benefit analysis.
Providing the scientific support to the regulatory department
Validate scientific claims made in any promotional material or reference checking
Develop content for promotional materials including visual aid, leave behind leaflets (LBLs), newsletter, website content, product monograph etc.
Carry out research to collect, collate and author reports highlighting the innovation and recent trends on specific therapeutic area. Search for recent trends in specific therapies in terms of products, procedures, newer safety/efficacy issues, dosing/regimen etc.
Collaborate and commnuicate with UPSA team in Medical Affairs, PV/Drug Safety, Regulatory, Legal/Compliance, Marketing/Commercial, Market Access/HEOR etc
Communicate updates, recent trends, reports with respective internal stakeholders.

Education & Experience

Master’s degree in Pharma
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3 to 8 years’) or equivalent combination of education, training, & experience.

Knowledge, Skills And Abilities

Strong understanding of pharmaceutical industry and regulatory services
Excellent scientific communication and presentation skills
Experience in medico marketing, healthcare marketing, or pharma consulting
Ability to translate scientific data into strategic marketing content
Strong client management and business development skills
Market research and competitive intelligence capabilities
Excellent PowerPoint presentation and documentation skills.

Location Gurgaon, Haryana (INDIA) _Onsite

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