Provide setup, configuration, administration, validation, reporting, and integration support for safety databases (e.g., Argus, Vault Safety, EDC). Collaborate with IT, QA, vendors, and clients to resolve technical issues, support handovers, drive process improvements, and ensure compliance with regulations such as 21 CFR Part 11 and EMA Annex 11. Role requires 2+ years of relevant experience, intermediate SQL, and familiarity with SDLC and change management.

Parexel is recruiting a Senior Scientific Specialist (1-year fixed-term, UK-based) with experience in HEOR and RWE to lead delivery of assigned programs, develop high-quality scientific content, manage client relationships, and mentor team members. The role requires advanced scientific writing/editing, project management, and proficiency in MS Office. Qualifications listed include a degree and higher degree in Life Sciences, Pharmacy, or Medicine (BSc/BA/PharmD/PhD/MD).

Lead preparation, review, and delivery of clinical trial transparency submissions (registrations, results postings, PLS/LPS, redaction/anonymization packages, reports, CCI justification). Provide regulatory interpretation and strategic guidance across ClinicalTrials.gov, EudraCT/CTIS, EMA Policy 0070, and Health Canada; mentor junior staff and manage complex disclosure projects.

Technical Writing Student internship supporting Daktronics manufacturing documentation: author, edit, format, and publish new and existing documents while working with engineers and product managers. Position is remote (home office) within the U.S. North Central region (MN, WI, IA); ~15 hours/week during academic year (up to 20), up to 40 hours/week in summer. Pay range $16–$19/hour. Applicants must be enrolled in an accredited bachelor’s program in a relevant field, submit transcripts and writing samples, be 18+, fluent in English, and eligible to work in the U.S.; employer does not sponsor visas.

Senior/Principal Medical Writer (remote, Poland) responsible for end-to-end development and QC of clinical study documents—protocols, IBs, ICF templates, DSURs, CSRs, and patient narratives—ensuring compliance with Precision MW style, SOPs, ICH/FDA/GCP guidance, clinical trial transparency and eCTD requirements. Role involves independent data interpretation, authoring complex content, contributing to SOPs/templates, performing literature research, and collaborating with sponsors, vendors, and internal teams. Minimum 5+ years’ senior medical writing experience (or 7+ years as Principal).

Senior/Principal Medical Writer responsible for planning, authoring, editing, formatting, and QC of clinical study documents (protocols, IBs, ICFs, DSURs, CSRs, patient narratives), ensuring compliance with Precision SOPs and regulatory guidance (ICH, FDA, GCP) and eCTD requirements. Requires a BS in a scientific/medical discipline and at least 5 years' experience as a senior medical writer (or 7+ years as principal), proficiency with Microsoft Office and Adobe Acrobat, and ability to collaborate with sponsors, vendors, and internal teams. Location: Remote (Slovakia).

Lead development and management of clinical study documents (protocols, IBs, ICFs, DSURs, CSRs, patient narratives) ensuring compliance with Precision style, SOPs, ICH/FDA/GCP, and eCTD. Perform writing, editing, formatting, QC review, literature-based research, and contribute to process/SOP/template maintenance. Requires BS in a scientific/medical discipline and 5+ years as a Senior Medical Writer (or 7+ years as Principal). Remote role based in Romania; candidates must be authorized to work without employer sponsorship.

Seeking a Senior/Principal Medical Writer to lead development of high-quality clinical study documents, ensure document lifecycle management with sponsors/vendors, perform QC and literature research, and contribute to SOPs/templates. Requires BS or equivalent in a scientific/medical discipline, proficiency with Microsoft Office/Adobe/Teams, and 5+ years (Sr. Medical Writer) or 7+ years (Principal) relevant experience; oncology/rare disease experience and advanced degrees are preferred. Candidates must be legally authorized to work in the country of employment without employer sponsorship.

The role leads development of high-quality clinical study documents from template to final approved version, collaborating with sponsors, vendors, and internal teams. Requires a BS (or equivalent) in a scientific/medical discipline, 5+ years' experience as a Senior Medical Writer (or 7+ as Principal), proficiency with Word/Excel/Teams/Adobe, knowledge of ICH/FDA/GCP, eCTD, and experience in oncology/rare disease preferred.

CrowdStrike is hiring a Technical Proposal Writer/Proposal Manager to manage end-to-end proposal activity (RFIs, RFPs, RFQs, DDQs, security questionnaires), coordinate SMEs, and produce compliant customer-facing responses. Remote role for East Coast US candidates; requires 3+ years managing complex proposals (experience in SaaS or cybersecurity preferred), proficiency with proposal platforms (RFPIO, Loopio, Responsive), Salesforce, MS Office/Google Workspace, and experience leveraging AI tools. Base salary range for U.S. candidates is $86,000–$135,000/year.

Senior technical leader responsible for defining and evolving the architecture and technical direction of GitLab's Core DevOps services (CI, CD, Plan, and source control). Role includes reducing systemic risk, driving convergence on shared patterns, integrating AI capabilities, mentoring senior engineers, participating in incident on-call, and delivering measurable reliability and performance improvements.

The role develops and edits clinical reference materials and continuing education (CE) modules for allied health, interprets and applies accrediting body requirements (e.g., ANCC, CA Board of RN), prepares and renews accreditation applications, leads content review cycles, analyzes learner data to improve content, and coordinates subject matter experts. Requires 7+ years of clinical writing/editing and accreditation experience.

Planful seeks an Associate Instructional Designer to design and build eLearning content—course guides, slide decks, hands-on labs, quizzes, and certification assessments—and keep the Academy catalog current as the product evolves. The role requires strong writing/editing skills, experience or coursework in instructional design (1–2 years), comfort with or willingness to learn authoring tools such as Synthesia, collaboration with SMEs and product teams, and use of AI-powered tools to accelerate development. The position is remote (Canada) and the listed base salary range is CAD 78,600–88,600 per year.

Founding architecture role in NVIDIA DGX Cloud Security Engineering responsible for defining and implementing the security design standard across a large GPU cloud platform (tenancy, workload isolation, identity, supply chain, detection). Hands-on seat leading a small team of Principal Engineers, interfacing with central security, and driving multi-year common security infrastructure. Requires substantial senior experience (posting references 18+ and typically 20+ years). Salary range provided: 320,000–488,750 USD base per year.

Responsible for preparing complete, customer-focused responses to procurement requests (RFPs, RFIs, RFQs) for FOLIO and related EBSCO SaaS solutions. Tasks include analyzing requirements, researching capabilities and library workflows, coordinating stakeholders across Sales/Product/Implementation/Support/Legal, managing timelines and deliverables, and maintaining reusable RFP content. Role requires 2+ years of relevant experience. Remote.

The Qualified Success Architect, University will own article updates and new article creation, develop best-practice content and partner certification paths, engage with the customer community, and partner cross-functionally with Product, Enablement, and CS to keep Qualified University content accurate and useful. Requires 3-7 years SaaS experience and prior customer success or customer education experience.

Parexel seeks a Scientific Specialist (6-month maternity cover, possible extension) based in the UK to develop and maintain high-quality scientific content (manuscripts, abstracts, presentations) focused on oncology. The role requires strong scientific writing, research, editing and project-management skills, collaboration with clients and external stakeholders, and an advanced degree in life sciences, pharmacy, or medicine.

Sysdig is hiring a Junior AI & Product Enablement Specialist to build and maintain hands-on lab scenarios and technical content (YAML/Markdown), script and automate training environments (Bash/Python), help troubleshoot platforms (e.g., Instruqt, LMS), and assist in delivering trainings and workshops. The role requires working knowledge of DevOps/cloud-native concepts, comfort with scripting and AI coding/agent clients, and working English. Location is flexible, listed as Spain and Costa Rica.

Create and maintain YAML/Markdown-based lab scenarios and courseware, script and automate parts of training environments using Bash or Python, and help troubleshoot delivery platforms (e.g., Instruqt, LMS). Assist in designing and delivering training sessions, demos and workshops, use AI coding/agent clients to accelerate content creation, and collaborate with cross-functional teams while developing teaching and presentation skills.

Work remotely in France on MongoDB's AMP team to shape architecture and lead modernization of legacy Java monoliths to cloud-native architectures using MongoDB. Responsibilities include assessment and decomposition of monoliths, relational-to-document data modeling, implementing production-quality Java/Spring Boot services, establishing CI/CD, automated testing, observability, and mentoring engineers. Professional fluency in French and approximately 8+ years of relevant Java application modernization experience are required.