Our Team

Narrative Director / Managing Medical Writer

With 25+years as a scientist and medical writer, Colleen has expertise in all phases of clinical writing, and leads Acumen’s narrative writing teams.

Managing Medical Writer

With a background as a research cancer biologist, Elin authors a wide range of nonclinical documents, both for regulatory and publications.

Lead Medical Writer

With a background in drug discovery, omics, and oncology, Dana has 17 years of experience as a research scientist, 10 years’ experience as a medical writer, and she supports clinical and non-clinical publications across a wide variety of therapeutic areas.

Lead Medical Writer

Nate is a veteran medical affairs professional specializing in medical affairs publication planning and content development.

Lead Medical Writer

Jacquie is a lead medical writer with over 18 years of experience writing clinical regulatory documents and publications.

Lead Medical Writer

With 18 years of medical writing experience, Dayna has deep experience writing regulatory documents, with a focus on oncology, rare disease, and gene therapy submissions.

Lead Medical Writer

Paula has led, written, and edited clinical, regulatory, and pharmacovigilance documents for more than 20 years with a strong focus on oncology.

Lead Medical Writer

Erin is a lead medical writer with a background in nonclinical writing for gene therapy programs. Erin also draws on her experience as a former analytical development scientist and technical compliance specialist for GMP testing and manufacturing.

Managing Medical Writer

As a lead medical writer for Acumen, Phil is able to bring his 20+ years of experience to clinical document preparation.

Lead Medical Writer

With 20 years of research experience in neuroscience and molecular biology, Pamela specializes in writing nonclinical and clinical publications and supports the development of regulatory documents.

Lead Medical Writer

With a background in immunology and cancer research, Jennifer has over 10 years of writing regulatory and clinical documents, with a focus on oncology.

Lead Medical Writer

With almost 20 years of experience researching, writing, and reviewing advanced concepts in biomedical sciences, Molly has expertise preparing nonclinical regulatory documents and publications.

Lead Medical Writer

With a background in immunology, molecular biology, and drug discovery, Petra contributes to a wide range of clinical documents.

Lead Medical Writer

Pat has 25 years of experience as a regulatory medical writer and has written a wide variety of clinical documents and contributed to many submissions.

Lead Medical Writer

In her nearly 20 years of experience as a medical writer, editor, and team leader, Courtneay has worked across multiple clinical document types and therapeutic areas.

Lead Medical Writer

Ava has been a medical writer for 15 years, with extensive experience in managing writing teams and overseeing processes. Ava also performs lead medical writing for all clinical document types.

Lead Medical Writer

Kathleen has over two decades of experience in publication planning and development, medical/scientific content, and advisory boards.

Senior Medical Writer

Caroline is an experienced research scientist who contributes to nonclinical and clinical writing and project management.

Senior Medical Writer

Joining Acumen after completing his PharmD, Aaron contributes to the development of various clinical documents including submission filings.

Senior Medical Writer

Alice is a medical writer with a cancer cell biology background who supports nonclinical publications and regulatory submissions.

Senior Medical Writer

Beth has been a medical writer for 17 years, with experience in multiple therapeutic areas and regulatory document types, including patient safety narratives.

Senior Medical Writer

With a background in molecular biology and over 10 years leading and managing research projects, Dikshya contributes to a wide range of clinical and nonclinical documents.

Senior Medical Writer

Ida is an experienced biochemist and applied microbiologist with a drug discovery background. She has additional experience in vaccinology and supports non-clinical and regulatory document writing.

Senior Medical Writer

Leveraging her background in molecular immunology and over 15 years of analytical experience, Jennifer authors both clinical and nonclinical regulatory documents and publications.

Senior Medical Writer

With over 10 years editing biomedical content, Lindsay supports both Acumen's clinical writing and editing.

Senior Medical Writer

Mary is a clinical writer with an extensive scientific background and experience across multiple regulatory document types, including patient narratives.

Senior Medical Writer

Mia is a medical writer and project manager with a background in pharmacology and translational science who supports clinical publications and regulatory submissions.

Senior Medical Writer

Paul is a medical writer with a focus on clinical manuscripts and publications, leveraging his extensive prior experience in academic publishing.

Medical Writer

Laney has 10 years of biomedical engineering research experience and contributes to Acumen’s clinical and non-clinical writing projects.

Medical Writer and Editor

Hilary leverages her background as a research scientist and project manager to support Acumen's writing and QC teams.

Narrative Medical Writer

Kris has over 20 years of pharma/biotech experience specializing in drug safety and narrative writing, having authored over 30,000 narratives.

Medical Writer

Sarah is a medical writer with experience in both basic science and clinical research. She supports clinical and nonclinical documents and publications.

Medical Writer

With a background as a research scientist, Sarah supports clinical and nonclinical documents.

CMC Regulatory Affairs Consultant/Writer

Darlene is a regulatory affairs and CMC writer with a background in CMC regulatory strategy; alongside Module 3 authoring, she performs risk mitigation and strategic CMC plans for biopharmaceutical companies.

Medical Writer

With a neuroscience background, Amanda supports clinical regulatory documentation.

Project Manager

Mandy leverages her background in biomedical engineering research to support project management and clinical writing at Acumen.

Project Coordinator

Rebecca contributes to Acumen’s software development and project management; she also supports Acumen’s narrative writing team as an editor and writer.

Regulatory Affairs Consultant

Katie is a Regulatory Affairs consultant with over 25 years of experience across devices, biologics, and drugs and a range of indications.

Regulatory Affairs Consultant and Senior Medical Writer

A strategic regulatory affairs professional and regulatory writer with over 30 years of experience in biopharmaceutical and device development. Expertise in FDA/MAA submissions, regulatory documentation, and navigating complex regulatory across a wide range of therapeutic areas, including oncology and immunology.

Clinical Trials Disclosure

Kim has 15 years of experience writing and reviewing clinical documents and managing global teams and has substantial expertise in clinical trial transparency and disclosure.