Write and develop scientific publications including manuscripts, abstracts, and posters for oncology products.
Review and ensure highest standards of content produced by junior team members.
Provide line management and mentorship to support team development.
Inizio is a strategic partner for health and life sciences, solving health challenges and developing transformational ideas. We are a team of 10,000 experts in 35 countries, fostering an inclusive and empowering culture.
Lead scientific strategy and content development for oncology medical communications programs.
Partner with senior scientific leaders and clients to translate complex clinical data into accurate, compelling communications.
Manage multiple projects, mentor junior team members, and ensure compliance with professional standards.
Our partner is a medical communications company that develops promotional medical education materials for oncology. They offer a flexible, collaborative remote work environment with a focus on scientific accuracy and evidence-based communication.
Develop scientific expertise in assigned therapeutic areas, supporting delivery for a versatile team.
Research and develop technical materials, ensuring accuracy and adherence to editorial style.
Communicate with clients and key opinion leaders on content development and attend scientific meetings.
Nucleus Global is a global leader in medical communications, part of the iNIZIO group, providing advisory, medical, marketing, and engagement services to life sciences companies. With over 900 employees across Europe, US, and APAC, it fosters a friendly and informal working environment with social events and wellbeing programs.
Research and develop technical materials ensuring accuracy and editorial style.
Partner with clients and KOLs on content development and attend scientific meetings.
Create materials for different medical audiences in various media formats.
ApotheCom is a leader in medical communications, providing high-quality medical communications programmes. As part of Inizio, a global healthcare consulting group with over 10,000 employees, they foster a diverse and inclusive workplace.
Plan, develop, and oversee scientific content for oncology accounts across multiple therapeutic areas.
Lead client interactions, brand strategy, and the scientific portion of brand planning and business development.
Manage resource allocation, develop SOWs, and identify areas for new and organic growth.
Lockwood collaborates with pharmaceutical, biotech, and medical device clients to develop science-based medical communication strategies. Over a third of its staff hold advanced scientific or medical degrees, and most work remotely, fostering a flexible, work-life balanced culture.
Provide strategic medical communication recommendations to support brand goals.
Lead execution of content development activities for oncology accounts.
Manage writing tasks including research, data-checking, and reference annotation.
Lockwood partners with pharmaceutical, biotech, and medical device companies to develop science-based medical communications strategies. Over a third of our staff hold advanced scientific or medical degrees, and our flexible remote structure supports work-life balance and attracts top talent.
Develop and write medically accurate content for a variety of resources, including value proposition slide decks, advisory boards, and internal training materials.
Serve as content point person on assigned accounts, ensuring high-quality work under limited supervision and strict timelines.
Collaborate with internal teams and pharmaceutical clients, attend medical/legal/regulatory review meetings, and mentor junior staff.
PRECISION AQ is a top payer marketing agency that supports global pharmaceutical and life sciences clients in commercial excellence. The company focuses on demonstrating the economic, clinical, and societal value of medical treatments to payers, providers, patients, and policymakers.
Lead scientific strategy and content development for oncology-focused medical communications programs.
Serve as a senior scientific partner to clients, driving brand planning and new business initiatives.
Manage multiple projects with rigorous editorial standards and cross-functional collaboration.
This role is listed on behalf of a partner company that provides AI-powered job matching services. Jobgether is a platform that uses AI to connect candidates with hiring companies, emphasizing efficiency and objectivity in recruitment.
Provide medical writing services and consultation to clinical research scientists and academic partners, including researching, writing, and editing scientific information.
Lead content planning and production of regulatory documents such as protocols, investigator brochures, and clinical study reports.
Act as primary contact and liaison with external publication executives and editors to coordinate content and revisions.
Alimentiv is a medical research organization providing medical writing services and consultation to clinical research scientists and academic partners. The company culture emphasizes continuous improvement and teamwork.
Lead scientific content planning and development for accounts across therapeutic areas.
Manage client interactions, brand strategy, and business development for scientific initiatives.
Requires 8+ years experience with promotional medical education and oncology expertise.
Lockwood collaborates with clients in pharmaceutical, biotech, and medical device industries to develop science-based medical communications strategies. Over a third of staff hold advanced scientific or medical degrees, and most work remotely for better work-life balance.
Lead the development of disease-state and product-specific materials and the omni-channel scientific communications strategy.
Oversee the development of standard and custom responses to unsolicited requests and create internal Medical Information resources.
Lead publication strategy and execution for clinical and nonclinical data including manuscripts, abstracts, posters, and presentations.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. The company is fully remote and headquartered in Radnor, Pennsylvania.
Lead scientific content planning and development for oncology accounts, overseeing brand strategy and client interactions.
Manage resource allocation, timelines, and SOWs in partnership with client services, driving organic growth.
Requires 10+ years of experience in promotional medical education, strong data analysis skills, and oncology expertise.
Lockwood collaborates with pharmaceutical, biotech, and medical device clients to develop science-based strategies through medical communications. Over a third of staff hold advanced scientific degrees, and most work remotely, fostering work-life balance and attracting top talent.
Set the strategic direction for scientific content across client accounts, ensuring alignment with client objectives and medical priorities.
Provide senior-level oversight and ensure quality, accuracy, and consistency of all deliverables.
Lead cross-functional teams, mentor junior staff, and contribute to business development through proposals and pitches.
Precision Medicine Group is a medical communications company that provides scientific content and strategy for pharmaceutical and biotech clients. They are known for award-winning work, strong client partnerships, and a commitment to professional development.
Develop and manage medical content for pharmaceutical, biopharma, and device clients, including SRDs, FAQs, and slide sets.
Drive document development from material gathering through MLR review, using tools like Veeva PromoMats.
Collaborate with global teams to ensure timely, high-quality, compliant deliverables that meet client needs.
EVERSANA provides next-generation commercialization services to the life sciences industry. With over 7,000 employees globally, the company serves more than 650 clients and is certified as a Great Place to Work, fostering an inclusive culture.
Lead development of complex medical writing and publication deliverables for clinical studies.
Define document strategies and coordinate writing activities across multidisciplinary teams.
Mentor less experienced writers and enhance processes to ensure high-quality outputs.
A global life sciences and healthcare company offering integrated services across the industry. It fosters an inclusive, collaborative culture focused on employee growth, professional development, and delivery of important therapies.
Lead author on complex regulatory and clinical documents including protocols, CSRs, IBs, and IND/NDA/BLA submissions.
Provide strategic input on document planning, messaging, and quality control while mentoring other writers.
Manage multiple projects independently, balancing timelines and client expectations in a fully remote environment.
Eldridge Writing provides top-tier medical writing services to pharmaceutical and biotechnology clients. We are a small, collaborative team that values quality and serves as a true extension of our clients’ teams.
Develop and execute publication strategies aligned with client objectives and evidence priorities across manuscripts, abstracts, posters, and congress activity.
Provide senior scientific oversight to ensure accuracy, clarity, and strategic alignment across deliverables including scientific platforms, core decks, and advisory board materials.
Serve as a senior scientific and strategic client contact, building trusted relationships and guiding content priorities and data interpretation.
Real Chemistry is a global healthcare communications and marketing agency that uses deep scientific expertise, human-centered creativity, and AI-driven insights to transform healthcare. The company is Great Place to Work certified and fosters a culture of collaboration and excellence.
Serve as scientific lead for client teams, ensuring content is evidence-based, accurate, and strategically aligned.
Analyze complex medical literature and mentor junior team members including Medical Writers.
Support business development, advisory boards, and regulatory review processes.
This partner company is a medical communications agency serving pharmaceutical and biotechnology clients. It offers a collaborative environment with opportunities for professional development and scientific leadership.
Prepares clinical and regulatory documents for drug and device development with moderate autonomy.
Coordinates review, approval, and quality control of clinical and regulatory projects.
Develops understanding of submission strategies, regulations, and project management to drive objectives.
AbbVie discovers and delivers innovative medicines and solutions for serious health issues across immunology, oncology, neuroscience, and aesthetics. The company is a global biopharmaceutical leader with a strong focus on research and development, employing thousands worldwide.
Develop high-quality, medically accurate promotional content for pharmaceutical clients.
Conduct literature reviews and manage multiple projects with strict deadlines.
Collaborate with multidisciplinary teams and mentor junior staff.
The company is a medical communications agency that supports pharmaceutical and life sciences clients with promotional and medical content. It fosters an inclusive and collaborative workplace committed to equal employment opportunity and professional growth.