Lead development of high-quality clinical study documents including protocols, IBs, ICF, DSURs, CSRs, and patient narratives.
Ensure smooth document management from template to final approval in collaboration with sponsors and internal teams.
Independently formulate key messages from clinical data and author complex content with impeccable attention to detail.
Precision Medicine Group is a precision medicine company that provides clinical, scientific, and operational services to support drug development. They are an Equal Opportunity Employer with a global team and a focus on innovation and quality.
Serving as medical point person on assigned accounts
Developing, writing and translating complex scientific data to a broad audience
Ensuring project quality and outcomes by demonstrating in-depth technical expertise
PRECISION AQ is a top payer marketing agency supporting global pharmaceutical and life sciences clients. The company offers training, mentorship, and a cross-functional project team environment.
Create high-quality medical affairs deliverables translating complex scientific data into clear, accurate content.
Collaborate with colleagues, clients, and external experts to shape audience-tailored materials aligned with client objectives.
Take ownership of projects from brief to delivery, ensuring scientific accuracy and engaging content.
Avalere Health is a healthcare agency focused on ensuring every patient is identified, treated, supported, and cared for. With major hubs in the US and UK, they emphasize inclusive culture, flexible work, and professional growth, supporting employee networks and family planning.
Develop and review medical response documents with scientific accuracy and editorial excellence.
Perform source-to-output verification, validate references, and ensure consistency across deliverables.
Support MLR readiness through quality checks aligned with FDA guidance, AMA style, and ICMJE standards.
EVERSANA creates next-generation commercialization services for the life sciences industry. Their global team of over 6,000 employees serves more than 670 clients, from biotech start-ups to pharmaceutical companies, and embraces diversity and inclusion.
Respond to drug information inquiries from healthcare professionals and patients, providing verbal or written responses.
Identify and intake adverse events and product complaints, ensuring compliance with regulatory requirements.
Translate documents and perform medical writing to support client communication and safety reporting.
EVERSANA provides next-generation commercialization services to the life sciences industry, helping bring innovative therapies to market. With a global team of over 6,000 employees, we serve more than 670 clients, from biotech start-ups to established pharmaceutical companies, and foster a culture of diversity and inclusion.
Author clinical study reports, protocols, informed consent forms, narratives, and investigator brochures across therapeutic areas.
Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines.
Mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict.
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, the company has a fast-growing, science-driven culture and is recognized as a Great Place to Work in 2021, among other awards.
Write clear and concise medical copy for HCPs and patients, adhering to ABPI guidelines and quality processes.
Collaborate with strategy, creative, and account teams to develop effective campaigns.
Manage projects from concept to completion, ensuring timelines and quality standards.
Real Chemistry is a global healthcare communications and marketing agency that partners with top pharmaceutical and biotech companies. The company fosters a culture of innovation and collaboration, with over 5 years of growth, and has been certified as a Great Place to Work.
Leads writing and preparing clinical and regulatory documents for drug and device development.
Coordinates review, approval, and quality control across functions to ensure compliance and timelines.
Develops knowledge of US and international regulations and participates in process improvements.
AbbVie discovers and delivers innovative medicines and solutions addressing serious health issues in immunology, oncology, neuroscience, and aesthetics. They are a large global biopharmaceutical company committed to having a remarkable impact on people's lives.
Produce high-quality content for diverse medical communications projects, demonstrating excellent scientific understanding.
Develop content with minimal supervision, within budget and on time, using client approval systems.
Attend conferences, present work to clients, and manage day-to-day client communication and relationships.
Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner, they bring together strategy, evidence, engagement, and technology to engineer breakthrough value.