Review and approve post-marketing Individual Case Safety Reports and Serious Adverse Event reports for medical assessment, including coding and causality.
Support signal detection activities, review aggregate reports like PBRERs and DSURs, and provide input for Risk Management Plans and regulatory responses.
Utilize advanced English and Japanese language skills to collaborate cross-culturally with global teams and clients, ensuring high-quality pharmacovigilance services.
Support a group of biopharmaceutical customers by understanding their business processes, providing guidance, and configuring the Vault Safety solution.
Act as a customer liaison, managing communication between implementation teams, stakeholders, and internal Veeva product teams to drive change management and adoption.
Collaborate with diverse stakeholders, shape ideas, enhance delivery models, and work closely with product management to communicate customer requirements and industry needs.
Veeva Systems is a mission-driven pioneer in industry cloud software, helping life sciences companies accelerate therapies to patients. As a fast-growing public benefit corporation with over $3B in annual revenue, it fosters a values-driven culture focused on customer and employee success with a flexible 'Work Anywhere' policy.
Translation of English documents into French or vice-versa.
Triage and respond to drug information inquiries from healthcare professionals and consumers.
Identify adverse events and product complaints during interactions with customers.
EVERSANA is a company that delivers next-generation commercialization services to the life sciences industry. They have a global team of more than 7,000 employees and serve more than 650 clients, ranging from innovative biotech start-ups to established pharmaceutical companies, fostering an inclusive and diverse culture.
Under the direction of a senior member of the team, assume leadership and functional representation for projects of low complexity assigned ensuring effective and rapid coordination and management of deliverables striving the team to meet the agreed targets and to comply with the agreed procedures, trackers and templates.
Perform quality control of regulatory intelligence screening of legislative requirements updates and ensure maintenance of the regulatory intelligence database and timely dissemination of pertinent changes.
Provide internal teams and Clients with expertise and guidance on national requirements.
Ergomed Group is a rapidly expanding global full-service mid-sized CRO specializing in Oncology and Rare Disease. The company includes the more specialised brands- PrimeVigilance, Adamas Consulting and Ergomed CRO and values employee experience, well-being and mental health.
Serve as the primary Medical Monitor for assigned clinical trials.
Lead ongoing clinical data review to ensure integrity, completeness, and scientific validity.
Provide strategic guidance across functions to optimize trial design, recruitment, and execution.
Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M in funding. They are a small, focused team where every person has direct impact — united by a shared commitment to care deeply, create boldly, and never stop learning.
Lead senior client relationships in Japan and act as the primary strategic advisor for local and global stakeholders.
Own the strategic narrative for Japan within global accounts, translating local market insights to influence global brand strategy.
Orchestrate Japan–global collaboration to ensure high-quality, compliant delivery of localized campaigns and assets.
Klick is an ecosystem of companies dedicated to realizing the full potential of people and clients in the life sciences industry. As a Best Managed Company with offices globally, it fosters a high-performance, people-first culture centered on creativity, collaboration, and impact.
Monitors all safety aspects of clinical research trials.
Collects, assesses and processes Adverse Events (SAE) for safety reporting.
Prepares narratives of adverse events for adjudication by the CEC.
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. At Cordis, teammates bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives.
Serve as the clinical lead for one or more clinical programs, with responsibility for clinical trial design, execution oversight, and delivery of key milestones.
Serve as medical monitor for assigned studies, including review of eligibility, protocol deviations, safety signals, SAEs/AEs, and benefit-risk assessments.
Contribute to global regulatory strategy and interactions with health authorities (FDA, EMA, PMDA, etc.).
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. They are a fully remote company headquartered in Radnor, Pennsylvania, with a culture that emphasizes collaboration and high-quality execution.
Triage medical inquiries and provide outstanding advice via email and phone to ensure patient safety and care.
Proactively engage with patients throughout their treatment journey, managing side effects and creating educational content.
Collaborate with clinical and support teams to build and improve processes and systems for high-quality, personalized healthcare.
Eucalyptus builds digital healthcare clinics, such as Juniper for weight management, across men's health, fertility, skincare, and preventative health. The company is a fast-growing, internationally-focused startup with over 350,000 patients and a motivated team that values high ownership and impact.
Conduct weekly multidisciplinary rounds with Midwest and West Coast care teams, reviewing patient goals and providing clinical oversight.
Serve as the designated reviewer for patient escalations, applying clinical judgment to prioritize and direct cases to appropriate next steps.
Alternate monthly care delivery education sessions with co-Medical Lead, developing and facilitating case-based learning for various roles.
Waymark is a mission-driven team transforming care for people with Medicaid benefits by partnering with communities, delivering technology-enabled, human-centered support. We're designing tools and systems that bring care directly to those who need it most – removing barriers and reimagining what’s possible in Medicaid healthcare delivery.
Design and scale programs that drive meaningful physician participation, sustained behavior, and monetizable insights.
Develop the insights strategy and design high-performing engagements, incentives, and targeting to deliver actionable outputs.
Build a scalable advisory board network and create differentiated physician experiences to drive content engagement and connect it to commercial outcomes.
Impiricus is the first and only AI-powered HCP Engagement Engine, designed to transform how life sciences companies support physicians by ethically connecting HCPs to pharma resources. It is a fast-growing company recognized by Deloitte, guided by a council of 2000+ trusted HCP advisors, and focused on delivering clinically meaningful, evidence-based resources to improve patient care.
Establishes and maintains relationships with healthcare entities, serving as an educational and informational resource.
Delivers fair-balanced clinical and scientific presentations to healthcare professionals and patient organizations.
Collaborates across multi-disciplinary internal groups to support medical/scientific and business objectives.
Shionogi Inc. is a pharmaceutical company that supports and represents its products with key opinion leaders, clinicians, institutions, and professional organizations. They focus on building long-term relationships and establishing rapport with healthcare professionals through scientific disease state and product discussions.
Help shape how AI understands and supports real-world clinical reasoning, patient interactions, and healthcare delivery.
Review, label, evaluate, and refine AI systems designed to support healthcare professionals and improve patient outcomes.
Work alongside AI researchers as part of an expert network matched to AI initiatives.
Aptura AI is building the next generation of clinically grounded AI. They partner directly with physicians to ensure these systems are safe, accurate, and aligned with real-world clinical reasoning.
Manage the end-to-end provider enrollment process to ensure all clinicians are fully vetted and ready for patient care.
Serve as the primary power user for CAQH ProView, managing profile data, re-attestations, and troubleshooting technical enrollment issues.
Investigate sanctions alerts and NPDB queries to ensure adverse findings are precisely documented and escalated.
Scan.com is a digital health scale-up making diagnostics accessible, fast, and transparent. The company is a profitable, high-growth startup with hundreds of patients served daily, backed by over $70M in VC funding and fostering an innovative, inclusive culture.
Develop and author Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs) per EU MDR to support regulatory submissions for CE Mark.
Conduct comprehensive literature searches, review scientific data, and critically appraise literature to support clinical evaluations and risk assessments.
Manage CEP/CER timelines using project management tools and serve as a subject matter expert for R&D and broader Clinical/Medical Affairs activities.
Intuitive is a pioneer and market leader in robotic-assisted surgery, focused on expanding the potential of physicians through minimally invasive care and intelligent technology. The company fosters an inclusive and diverse team of passionate people grounded in integrity, with a strong capacity to learn and the energy to get things done, actively investing in long-term team member growth.
Review and validate translations of user-facing documents.
Ensure translations adhere to XUND’s tone and style guide.
Identify grammar, spelling, or terminology issues and make corrections.
XUND is a leading digital health scale-up that enables healthcare companies to digitize patient interactions and translate data into actionable insights. They aim to improve healthcare quality and accessibility by uniting medicine, technology, and a human-centered mindset.
Part of the Veeva Development Team within the Information System organization.
System administrator in the Veeva Quality and Regulatory systems.
Hands-on role combining system administration, configuration, solution design, and system evolution within the Veeva Development Cloud ecosystem.
Sobi redefines the standards of care and transforms the lives of people living with rare diseases. They are a diverse team of entrepreneurial people, with over 1,900 employees in more than 30 countries, passionate about growth towards becoming a global leader.