Real World Analytical ResearcherKMK Consulting Inc. • Morris Plains, NJ, US
Real World Analytical Researcher
KMK Consulting Inc. • Morris Plains, NJ, US
[job_card.variable_days_ago]
[job_preview.job_type]
- [job_card.full_time]
[job_card.job_description]PharmD from a US-accredited program or equivalent pharmacist training. In-depth knowledge and working experience of US health care system and coding systems. Ability to summarize drug classes, mechanisms of action, indications, clinical data, and therapeutic area insights across both familiar and unfamiliar domains. Strong literature search skills, including evidence extraction, critical appraisal, and synthesis of scientific findings. Ability to independently review peer-reviewed publications, guidelines, and databases to generate accurate scientific insights. Demonstrated experience developing high-quality scientific documents such as slide decks, abstracts, posters, or review summaries. Strong ability to distill complex data into clear, engaging, and scientifically sound content. Advanced PowerPoint skills for developing visually compelling scientific presentations. Proficiency in Excel, including pivot tables and basic analysis. Familiarity with AI-based tools used for literature searching, review, or summarization. (Preferred but not required) Basic skills in SAS, R, SQL, or Python for data review, extraction, or workflow enhancement. Excellent written and verbal communication skills. High learning agility, strong problem-solving ability, and adaptability to new therapeutic areas and project types. Ability to work independently and collaboratively in a fast-paced, project-driven environment.
Job Description
Overview
This is a US based full-time role supporting a global pharmaceutical company’s Innovative Scientific and Analytics function. Both NJ and remote based candidates are equally considered. This role is ideal for a PharmD or pharmacy trained professional with strong scientific research capabilities, medical writing expertise, and the ability to work across diverse therapeutic areas. The position involves reviewing scientific literature, developing high-quality medical and scientific content, collaborating with cross-functional teams, and supporting evidence-generation and strategic insights projects.
Key Responsibilities
- Conduct comprehensive literature reviews, analyze scientific publications, treatment guidelines, payer documents and clinical data, and emerging research.
- Develop high-quality scientific content, including slide decks, abstracts, posters, written summaries, payer documents and other medical communications deliverables.
- Collaborate with business stakeholders to identify, review and classify drug and study codes (ICD, NDC, HCPCS, etc.) to support real world analytics and research
- Translate complex clinical and scientific information into clear, concise, and accurate materials tailored to scientific, medical, or internal stakeholder audiences.
- Collaborate with cross-functional teams—including scientific strategy, analytics, and commercial insights—to support evidence generation and research initiatives.
- Ensure accuracy, consistency, and alignment with scientific standards, project objectives, and client expectations.
- Manage timelines and deliverables across multiple concurrent projects while maintaining strong attention to detail and scientific integrity.
- Adapt quickly to new therapeutic areas and project types as needed.
Qualifications
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