Develop Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs) per EU MDR to support CE Mark submissions.
Interact with cross-functional teams to define strategies for clinical documentation and regulatory submissions.
Conduct literature searches, critically appraise scientific data, and write clinical summaries for products and surgical procedures.
Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, developing technologies like the da Vinci surgical system and Ion to transform surgery. The company is a team of engineers, clinicians, and innovators united by a purpose to make surgery smarter, safer, and more human, with challenging but deeply meaningful work.
Develop high-quality, scientifically robust content across Oncology-focused medical communications projects.
Transform complex scientific data into clear, engaging narratives for healthcare professional audiences.
Provide editorial oversight, strategic input, and build strong relationships with clients and experts.
Avalere Health is a global healthcare advisory, medical, and marketing services company dedicated to ensuring every patient is identified, treated, supported, and cared for. They foster an inclusive culture with Employee Network Groups, flexible working, and a commitment to diversity and inclusion.
Craft and review regulatory documents such as clinical study reports, protocols, and investigator's brochures.
Collaborate with a supportive team to exceed client expectations.
Learn the intricacies of drug development and the science behind pharmaceuticals and biologics.
Eldridge Writing is a growing firm providing top-tier medical writing services to pharmaceutical and biotechnology clients. They pride themselves on quality and mentorship of the next generation of medical writers.
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.
Edit and review informed consent forms to ensure regulatory compliance and clarity.
Collaborate with IRB members, sponsors, and sites to incorporate required language.
Mentor junior editors and contribute to process improvements for quality control.
The partner company provides specialized services for clinical research and regulatory compliance. It fosters a collaborative environment and emphasizes ethical research practices, though team size is not specified.
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.
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.
Develop and deliver multiple oncology publications including manuscripts, abstracts, posters, presentations, and congress materials.
Interpret and communicate complex clinical and scientific data accurately with authors and subject-matter experts.
Manage multiple projects and deadlines across a busy account while applying publication guidelines and ethical standards.
ApotheCom is a global medical communications agency that partners with pharmaceutical and biotech companies to translate complex science into compelling communications. They have a collaborative, inclusive culture and value scientific expertise.
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.
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.