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.
Help build your dream AI-enabled authoring platform by guiding product and engineering teams on source data mapping, document logic, and summary execution.
Define document generation frameworks for regulatory-grade documents, starting with clinical trial results and scaling to broader submissions.
Establish objective quality criteria, review protocols, and verification frameworks to ensure outputs meet global regulatory expectations.
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, surpassing $3 billion in revenue, we are a public benefit corporation with a flexible work environment and a commitment to employee success.
Lead content development for multiple projects, ensuring high quality and adherence to regulatory guidelines.
Collaborate with internal teams and external stakeholders to develop strategic medical communications.
Supervise medical writers and contribute to new business proposals and pitch meetings.
PRECISION AQ is a top payer marketing agency that supports global pharmaceutical and life sciences clients in achieving commercial excellence. We are a specialized agency with a focus on improving market access, fostering a collaborative and detail-oriented culture.
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.
Create bioanalytical reports, plans, and submission documents in support of internal projects and regulatory preclinical/clinical studies.
Extract and format data from multiple lab systems for integration into reports using Microsoft Office.
Ensure documentation complies with FDA, GxP, EMA, and other regulatory guidelines.
BioAgilytix provides best-in-class bioanalytical services to support new medicine breakthroughs. They have a team of highly experienced scientists and professionals, are growing, and are committed to being solution-oriented and deadline-driven.
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.
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.
Serve as subject matter expert defining gold standard for AI-generated clinical content.
Share knowledge about day-in-the-life working with data for regulatory submissions.
Identify realistic sources of variance or data corruption in study data.
Edison Scientific builds and commercializes AI agents for science to accelerate scientific discovery. They are assembling a small team of top researchers and engineers across AI and biology to build an AI scientist.
Author comprehensive user operations guides for five immunization data systems.
Translate complex technical and clinical concepts into plain-language instructions.
Ensure all deliverables meet Section 508 accessibility standards.
Akicita Federal provides technical and business support services to government clients, including the Indian Health Service. They are a small business focused on federal IT and healthcare projects, with a collaborative culture.
Provide regulatory advice and ensure compliance with U.S. regulations and ICH GCP guidelines for clinical research sites.
Coordinate IRB submissions, maintain regulatory documentation, and support site start-up and close-out activities.
Collaborate with cross-functional teams and monitor regulatory changes to advise stakeholders.
Care Access is working to make the future of health better for all by bringing world-class research and health services directly to communities that often face barriers to care. With hundreds of research locations, mobile clinics, and clinicians across the globe, the company is dedicated to ensuring every person has the opportunity to understand their health and contribute to medical breakthroughs.
Write, edit, and proofread executive-level communications products for VHA senior leadership.
Develop educational materials and digital assets that promote awareness of suicide prevention initiatives.
Ensure all materials adhere to VA branding guidelines, Section 508 accessibility, and plain language principles.
Artemis supports the Veterans Health Administration (VHA) in public and mental health communications. The company operates with a focus on government contracts and employs a team of professionals dedicated to providing superior service.
Provide study oversight as primary liaison between CRAs, internal staff, site staff, client personnel, and external vendors.
Ensure clinical monitoring activities comply with SOPs, regulations, GCP, KPIs, and study-specific requirements.
Develop and manage clinical plans and guidelines, including the clinical monitoring plan and study timelines.
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996, supporting research behind innovative treatments in pharmaceutical, biotech, and medical device industries. They foster a collaborative community where team members feel valued, supported, and empowered to make a meaningful impact on global health.
Oversee clinical site management and ensure compliance with protocols, regulations, and quality standards.
Serve as primary contact for study sites, conducting monitoring visits from pre-study through close-out.
Collaborate with cross-functional teams to support data review, regulatory submissions, and site performance.
Our partner is a global clinical research organization managing monitoring activities across Phase I–IV trials and Real World Evidence studies. It offers a collaborative, fully remote environment focused on improving patient outcomes with professional growth opportunities.