Real World Analytical Researcher

KMK Consulting, Inc.•Morris Plains, NJ

7d•Remote

About The Position

KMK is a global data analytics and technology consulting company empowering leaders across the Life Sciences industries to make better data-driven decisions. Our data analytics and software platforms support data science, commercial operations, real world evidence, and cloud information management. We help to optimize business strategy and operations by delivering cutting edge analytics from the broadest set of data sources, combined with deep technical and domain expertise. We enable commercial excellence delivering analytical guidance to the field through SalesOps™, our cloud-based sales planning and operations platform. We are leaders in managing data using the latest cloud information management and big data technologies. We have more than 220 employees worldwide, are growing rapidly, and are proud to count a number of the top 10 global Life Sciences companies as our customers. We serve clients with a high-touch on-site and onshore presence, leveraged by a global delivery platform. 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.

Requirements

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.
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.

Nice To Haves

Basic skills in SAS, R, SQL, or Python for data review, extraction, or workflow enhancement.

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.

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