Source Job

• 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.

• 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 the preparation of complex clinical and regulatory documents including Clinical Study Protocols, Clinical Study Reports, and Investigator Brochures.
• Collaborate with clinical development teams and stakeholders to produce accurate, compliant, and scientifically robust documentation.
• Manage document timelines, review cycles, and project deliverables while ensuring quality standards and regulatory requirements are met.

Our partner is a specialized medical writing team supporting the development of high-quality regulatory documentation for the global pharmaceutical industry. It offers a collaborative, remote environment focused on quality, precision, and scientific communication.

• Develop high-quality clinical and regulatory documents supporting global submissions
• Partner with cross-functional teams to transform complex scientific data into clear narratives
• Ensure compliance with regulatory requirements while managing document timelines

Acadia Pharmaceuticals is a biopharmaceutical company developing innovative therapies to address unmet medical needs in neuroscience. With a collaborative and patient-focused culture, the company is committed to advancing treatments that improve lives.

• 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.

• Develop high-quality, evidence-based medical content for healthcare professionals that supports clinical integrity and commercial objectives.
• Translate complex scientific information into clear, compelling communications across print and digital formats.
• Collaborate with cross-functional teams including medical, legal, and design to manage multiple projects and meet timelines.

Montu is Australia's largest healthtech business focusing on alternative healthcare, supporting patients, doctors, and pharmacies. Founded in 2019, Montu has been recognized as Australia's fastest-growing tech company with a driven and results-focused culture.

• Independently plans and prepares regulatory documents and medical communications for all phases of product development.
• Organizes, analyzes, interprets, and presents scientific and statistical information per ICH guidelines.
• Collaborates with cross-functional internal and external document production teams.

Veristat is a global contract research organization with over 30 years of expertise accelerating life-changing therapies to patients worldwide. The company has a flexible, inclusive culture with a 70% remote workforce and 66% women-led teams.

• Independently plans and prepares regulatory documents and medical communications to support all phases of product development.
• Organizes, analyzes, interprets, and presents scientific and statistical information in accordance with industry guidelines (ICH, ICMJE, GPP).
• Collaborates with cross-functional internal and external teams under direction of Medical Writing management.

Veristat is a global contract research organization that accelerates life-changing therapies to patients worldwide. With over 30 years of expertise, the company has supported more than 105 approved therapies and fosters a flexible, inclusive culture with 70% remote workforce and 66% women-led teams.

• Critically evaluate scientific literature and produce accurate regulatory documents.
• Manage writing assignments across multiple projects and ensure timely delivery.
• Work directly with clients and multidisciplinary teams on regulatory submissions.

A partner company in the pharmaceutical, biotechnology, and medical device sectors is hiring a Senior Medical Writer. The company offers a fully remote environment and opportunities to work on a broad portfolio of clinical and regulatory documents.

• 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 scientific content for brand goals.
• Engage with KOLs and HCPs while managing resources and timelines.
• Conduct background research, data-checking, and reference annotation.

Lockwood collaborates with pharmaceutical, biotech, and medical device clients to create holistic, science-based medical communication strategies. Over a third of staff hold advanced degrees, and most work remotely, fostering a flexible structure and work-life balance.

• 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.

• 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.

• Collaborate with physician advisors to help medical school applicants draft, revise, and edit personal statements, activities sections, and secondary applications.
• Provide guiding questions and suggestions to ensure essays have logical flow, and edit for clarity, tone, syntax, grammar, and word choice.
• Maintain a supportive environment for applicants, offering relevant and actionable feedback through multiple revision cycles.

MedSchoolCoach is a rapidly growing EdTech company that provides content, software, and one-to-one tutoring and advising services for future physicians. They are a distributed team of creative, approachable, and motivated entrepreneurs, educators, tutors, advisors, and clinicians passionate about improving healthcare and education.

• 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.

• Build and maintain scientific relationships with healthcare professionals and medical experts.
• Gather and communicate medical insights to inform research and strategy.
• Collaborate with cross-functional teams to support evidence-based discussions and healthcare initiatives.

The company is a healthcare organization focused on advancing innovative therapies and improving patient outcomes. While the specific size is not disclosed, the culture is collaborative, inclusive, and supportive of professional growth.

• Serves as regulatory document specialist for clinical trial start-up, maintenance, and close-out.
• Collects, reviews, and maintains essential documents in the electronic Trial Master File (eTMF).
• Communicates with study teams and sites to ensure regulatory files remain complete and inspection-ready.

St. Jude Children’s Research Hospital is a leading research and treatment center focused on pediatric catastrophic diseases. It is a large institution with a collaborative culture and a strong emphasis on finding cures and saving children.