Own the strategic scientific narrative for a lead program, building fluency in science, data, development strategy, competitive context, and patient value.
Shape scientific positioning and key messages in critical clinical and regulatory documents, including protocols, IBs, CSRs, briefing docs, and overviews.
Serve as a connective thread across Clinical Development, Regulatory Affairs, Medical Affairs, Commercial, and other functions to ensure a consistent, rigorous scientific story.
Lead and develop a high-performing regional MSL team, fostering a culture of scientific excellence and continuous improvement.
Translate medical strategy into field execution and oversee territory planning to maximize impact with external experts.
Collect and synthesize field insights to inform clinical development, medical strategy, and educational initiatives.
Jobgether is an AI-powered job matching platform that connects top candidates with hiring companies. It is a dynamic, mission-driven organization dedicated to efficient and fair recruitment processes.
Lead integrated publication strategies and scientific communications for Kardigan's cardiovascular portfolio.
Oversee publication governance, compliance, and medical information operations.
Collaborate cross-functionally to translate scientific evidence into congress presentations and resources.
Kardigan is a heart health company developing targeted treatments to make cardiovascular disease preventable and curable. It has an industry-leading team and a culture driven by patients, authenticity, and curiosity.
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.
Lead the development of messaging and narratives that make complex research-driven work clear, accurate, and compelling.
Own end-to-end responsibility for an emerging strategic communications function within a rapidly growing organization.
Translate research, funding decisions, and ideas into communications tailored to different audiences, channels, and contexts.
This organization is a mission-driven entity focused on maximizing positive impact through rigorous research and effective resource allocation. It is a rapidly growing organization with a collaborative culture centered on transparency, truth-seeking, and intellectual rigor.
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.
Provides strategic and scientific leadership for patient-centered outcomes engagements, ensuring research design and evidence packages are fit-for-purpose.
Owns client relationships, drives business development, and leads proposal development to achieve revenue and sales targets.
Oversees clinical outcome assessment projects including literature reviews, gap analyses, regulatory strategy, and dossier development.
Lumanity is a global strategic partner that brings together strategy, evidence, engagement, and technology to improve health outcomes. The company is dedicated to accelerating and optimizing access to life-changing medicines.
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 and develop a high-performing field medical team focused on impactful scientific engagement within the neuroscience and mental health community.
Translate medical strategy into effective field activities, overseeing MSL operations across a defined region.
Drive execution of the national medical affairs plan and coach MSLs to enhance scientific credibility and performance.
Compass Pathways is a biotechnology company dedicated to unlocking new treatment options in mental health care, focusing on developing COMP360 psilocybin for treatment-resistant depression and PTSD. The company is headquartered in London with a US office in New Jersey, and leads the world's largest classic psychedelic clinical program.
Develop and lead integrated global regulatory strategies for I&I pipeline programs.
Serve as primary regulatory strategist and Health Authority relationship lead.
Provide expert guidance on development plan design and filing strategies.
Beeline Medicines is a clinical-stage biotechnology company developing precision therapies for autoimmune and inflammatory diseases. It is a small company backed by world-class investors, with a culture of scientific rigor and operational excellence.
Define and lead global regulatory strategy for clinical-stage radiopharmaceutical programs.
Lead key regulatory submissions including INDs, CTAs, and DMFs.
Serve as primary contact for regulatory agencies and build strong relationships with health authorities.
ARTBIO discovers and develops a new class of Alpha Radioligand Therapies (ARTs) to redefine cancer care. It is a global biotech with offices in Boston, Basel, London, and Oslo, fostering a collaborative and supportive culture.
Lead the clinical development strategy for AL137, owning the medical strategy for Phase 1 and shaping the path toward later-stage development.
Provide medical leadership for protocol design, safety considerations, dose escalation, and data interpretation in early clinical trials.
Serve as the internal physician expert, integrating AI technologies to accelerate analysis and improve decision-making.
Alector develops therapies that empower the immune system to combat neurodegeneration. The company is supported by experienced scientists, leading healthcare investors, and pharma partners, fostering a dynamic and flexible culture that encourages experimentation and ownership.
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.
Develop and execute a comprehensive PR and communications strategy aligned to business goals.
Elevate market-facing attorneys as thought leaders through messaging and visibility plans.
Establish media relationships and drive thought leadership content including articles and speaking engagements.
Envoy Global is a proven innovator in the global immigration space, combining a tech platform with holistic service. The company is growth-oriented and seeking to build its communications function from the ground up.
Lead the Scientific Program Management function, establishing practices, standards, and operating rhythms for program execution.
Partner with scientific and organizational leadership to align program priorities, manage risks, and provide portfolio visibility.
Directly manage and develop a team of Scientific Program Managers, fostering a culture of collaboration and continuous improvement.
Sage Bionetworks is a nonprofit that uses open science and collaboration to improve human health. They are a mission-driven, distributed team of scientists, engineers, and governance experts.
Define and drive asset strategy for small molecule clinical programs in oncology and immunology/inflammation, integrating competitive positioning and biomarker strategy.
Translate Recursion OS and ClinTech insights into strategic advantages, ensuring proprietary data and computational insights maximally enable drug discovery and development.
Partner with functional leaders across clinical development, BD, finance, and platform teams to align resource allocation with strategic conviction and impact.
Recursion is a clinical-stage TechBio company decoding biology to improve lives, advancing a pipeline of investigational medicines across oncology, rare disease, neuroscience, and immunology. The company uses its AI-native Recursion OS platform and employs a team fluent in both science and AI, with offices in Salt Lake City, Oxfordshire, New York, Montréal, and London.
Lead medical and scientific review of promotional and non-promotional materials for assigned products and markets.
Ensure scientific accuracy, regulatory compliance, and fair balance in content, collaborating with cross-functional teams.
Develop and review medical content, including scientific narratives and medical information, adhering to industry standards.
EVERSANA provides next-generation commercialization services to the life sciences industry, helping bring innovative therapies to market. With over 7,000 employees globally, they serve more than 670 clients and are certified as a Great Place to Work.
Lead risk management and safety data review for assigned products, ensuring regulatory compliance.
Provide safety-related content for clinical and regulatory documents, and prepare for inspections.
Mentor a small pharmacovigilance team while driving end-to-end operational oversight.
Orca Bio is a commercial-stage biotechnology company redefining the transplant process by developing next-generation cell therapies for blood cancer patients. We maintain a start-up culture of camaraderie and leadership by example, with a small dedicated team.
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.
Own regulatory review and approval of promotional materials across HCP, DTC, digital, and social channels, ensuring compliance with FDA regulations.
Partner with Commercial, Medical Affairs, and Legal to shape campaigns and claims, providing clear guidance to reduce approval delays.
Lead FDA promotional submissions, monitor regulatory trends, and build scalable processes to support product launches.
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders. The company values Trust, Ownership, Curiosity, and Results, and offers a collaborative, high-achieving environment with a focus on diversity and inclusion.
Own Later's PR and communications strategy, aligning press narratives with corporate and product priorities across all three business lines.
Build and maintain relationships with tier-1 press, secure earned media, and draft press materials.
Partner with Product Marketing, Content, Executive Leadership, and external PR firm to drive high-impact coverage.
Later is the world's most intelligent influencer marketing company, combining real creator relationships, trusted intelligence, and expert guidance to help brands create unforgettable campaigns. Trusted by leading enterprise brands including Nike, Wayfair, Unilever, and Southwest Airlines, Later fosters a culture rooted in an inclusion-first mindset with a focus on diversity and equity.