At Catawiki, every day brings the extraordinary! Whether it’s Daniel Ricciardo’s Formula 1 Car, a Woolly Mammoth’s Skeleton, Lady Gaga's Jumpsuit or Usain Bolt’s running shoe, we encounter exceptional objects every day. We’re a one-of-a-kind marketplace for buying and selling special objects. Each week, more than 110,000 unique items are auctioned, all carefully curated by our passionate in-house experts. Having sold over 25 million unique objects, our mission is to become the world’s most popular destination for special objects. As a growing, diverse and sustainable scale-up, we proudly live by three core values. If these values resonate with you, we’d love to explore how you can join us. - Taking ownership and driving impact - Being open to change and feedback - Being passionate about our mission and our customers. Your Mission As a Model Cars Expert, you will curate high-quality auctions that attract engaged bidders and trusted sellers. Your expertise ensures each lot, whether vintage or recent, is relevant, accurately valued, and aligned with collector expectations. You contribute directly to the growth and success of your category by combining specialist knowledge with commercial judgement, maintaining transparency and building strong relationships within the model cars community. What You’ll Do - Evaluate and arrange model car lots submitted by users, ensuring each auction features attractive and relevant listings - Create compelling weekly lot selections using your expertise and professional network - Review titles, descriptions, and images to assess quality and provide accurate estimated values - Safeguard transparent and fair transactions through consistent expert evaluation - Communicate rejections professionally and diplomatically, maintaining strong seller relationships - Collaborate with Sales to attract new sellers and diversify the range and quality of lots - Partner with Marketing to increase bidder engagement and visibility for your auctions What You’ll Bring - Expert knowledge in Model Cars, both vintage and recent - Strong commercial acumen and documented commercial experience - An eye for trade and value within the collectibles market - Excellent communication skills, with the ability to act diplomatically in user disputes - A network of potential sellers and experts within your field - Good computer skills and confidence working with digital tools - Good command of English, written and spoken Where You’ll Be This is a 100% remote role that can be based in the Netherlands, Belgium, France, Germany, Italy, Portugal, Spain, or the United Kingdom. Why You'll Love Working with Us - Create a visible impact by working at scale in a global organisation serving millions of customers across 80+ categories. In our flat structure, every role has a broad scope and directly impacts both our customers and the business. - Learn and grow through our Learning & Development initiatives, including clear development plans and mentorship programmes to support your career progression. - A culture of connection defines us. We’re a passionate, diverse team of 800+ Catawikians representing 60+ nationalities. We foster an inclusive and queer-friendly environment where everyone is encouraged to bring their full self to work. - Celebrate life’s moments with us. You’ll receive a €100 Catavoucher when you join, a €50 Catavoucher on your birthday, and an extra day off each year to “Pursue Your Passion”. We also offer additional leave for key work anniversaries and important life events. Benefits may vary by location. Our Offices and Way of Working Our vibrant offices in Amsterdam, Paris and Lisbon are designed to inspire collaboration. Most Catawikians operate in a hybrid setup, combining office-based and remote work, with a minimum of two days per week in the office, unless a role is explicitly stated as fully remote or fully office-based. Interested? Apply with an English CV and Cover Letter. By applying, you agree to Catawiki’s Applicant Privacy Policy. If you’re excited about this role but don’t meet every requirement, we still encourage you to apply anyway. You may be just the right candidate for this or other roles.

Senior Director, Global Pharmacovigilance - Safety Physician Location: Remote, US Job Description: Vacancy No VN756 Employment Type Full Time Department Regulatory Affairs Key Responsibilities The Senior Director, Global Pharmacovigilance (Safety Physician) is a senior medical leader accountable for the global medical safety strategy, benefit-risk assessment, and risk management of Immunocore's development and marketed products. The role holder is a board-certified physician and recognized subject matter expert in pharmacovigilance, with deep experience in biologic product safety, signal detection, epidemiology, and regulatory benefit-risk decision making (e.g., FDA, EMA and other Health Authorities), providing strategic and operational leadership across all phases of the product lifecycle from early development through post marketing. Key aspects of the role include leading proactive, data driven benefit-risk assessment and advanced signal detection using clinical trial, post marketing, and real world data; shaping and executing global Pharmacovigilance Plans and Risk Management Plans, including the design and interpretation of post authorization safety and active surveillance studies; directing and developing a team of pharmacovigilance physicians and safety professionals by setting strategy, building capabilities, and embedding best practices aligned with Immunocore's Senior Director career framework; and serving as the senior medical safety authority for assigned products, representing Immunocore in high level interactions with global Health Authorities and external partners. KEY RESPONSIBILITIES - Develop and implement global pharmacovigilance strategies for assigned products, aligned with clinical, regulatory, and commercial objectives. - Lead ongoing benefit-risk assessments using data from clinical trials, post marketing surveillance, real world data sources, and epidemiologic/active safety studies. - Oversee systematic signal detection and evaluation from Individual Case Safety Reports, aggregate/periodic reports, literature, and other data sources. - Direct the design, conduct, and interpretation of active safety surveillance and pharmacoepidemiology studies to characterise and quantify product risks. - Lead multidisciplinary Safety Management/Safety Review Teams to drive signal evaluation, surveillance strategies, and risk mitigation recommendations. - Be accountable for the medical and scientific quality of aggregate safety reports, Pharmacovigilance Plans/RMPs, Investigator's Brochures, and safety sections of regulatory submissions. - Provide senior medical safety leadership for global regulatory submissions and labelling negotiations, and respond to Health Authority queries on product safety, benefit-risk, and risk management. - Provide senior level oversight of medical review of ICSRs, ensuring accurate assessment of causality, seriousness, expectedness, and clinical relevance. - Guide internal teams and external vendors/CROs on best practices for safety data collection, coding (e.g., MedDRA), evaluation, and use of safety databases and analytics tools. - Serve as the senior safety representative on cross functional clinical and project teams, ensuring integrated safety input into study design, protocols, analyses, and portfolio decisions. - Champion cross functional collaboration and engagement with external stakeholders to shape Immunocore's safety strategy and external scientific profile. - Lead continuous improvement of PV processes, SOPs, and tools, and maintain current knowledge of evolving pharmacovigilance and biologic safety guidance. SUPERVISORY RESPONSIBILITY This position will not have line manager responsibilities, but provides safety leadership to cross functional teams EXPERIENCE & KNOWLEDGE Essential - Experience with concepts of signal detection and review of aggregate data to identify potential emerging safety issues, benefit risk assessment, and risk management strategies. - Experience in the preparation and contribution to authoring of aggregate safety reports for regulator submission. - Knowledge of clinical development process - Demonstrated ability to prioritise multiple tasks and deliver to deadline with high standard of quality. - Demonstrated track record in Authoring or overseeing aggregate safety reports (DSURs, PSURs/PBRERs, PADERs) and contributing to major regulatory submissions (e.g., BLA, MAA) and subsequent labelling updates. Desirable - Advanced degree in epidemiology, pharmacology, or biomedical sciences (PhD/MPH) - Knowledge of drug approval process in major countries - Experience with different commercially available safety databases. - Board certification in a relevant specialty - Experience with global product launches and implementation/assessment of complex risk minimisation measures. - Evidence of scientific contributions to the field (e.g., peer reviewed publications, invited presentations, guideline development, or recognised subject matter expertise in biologic safety). EDUCATION & QUALIFICATIONS - M.D./D.O. degree with at least five years of pharmacovigilance experience, and at least two years of clinical experience or relevant experience to understand clinical drug development - At least five years of practical clinical experience post licensure US Salary Range $187,500-$312,000 About the Company Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry's most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions. Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases. At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients' lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law.

Oversee a team managing risk-related activities, develop and implement risk management strategies, monitor risk indicators, and collaborate with stakeholders to enhance operational efficiency and mitigate potential risks.

Title: Production Professional Location: Louisville, KY, United States Employee Type: Contract Remote: Yes Job Type: Pay Range: $39 - $40 per hour Job Description: Job#: 3031003 Job Description: Job Title: Professional 2, Production Assignment Length: 12 months Work Location: Remote Job Summary The Professional 2, Production role supports the production of a wide range of print materials for both internal and external audiences. This position works on varied assignments that require independent judgment, interpretation of requirements, and selection of appropriate production approaches. This role partners closely with internal stakeholders and external vendors to ensure high quality, timely delivery of print materials. The individual is expected to work with minimal supervision and exercise sound judgment while adhering to established standards and procedures. Key Responsibilities Produce and manage print projects for internal and external audiences Support preformatted and recurring publications such as quarterly reports Coordinate with printers, designers, and other external vendors Provide guidance and recommendations on production techniques and processes Consult with internal clients to ensure production needs are clearly understood and met Apply strong judgment in selecting work methods, including in situations with limited direction Demonstrate understanding of departmental and organizational goals and how work supports broader objectives Ensure all deliverables meet quality standards, deadlines, and style guidelines Required Qualifications Bachelor’s degree required Less than five years of relevant technical or production experience Strong written and verbal communication skills Excellent grammar and proofreading skills with proficiency in Associated Press style High attention to detail and accuracy Ability to manage multiple deadlines effectively Strong interest in contributing to an organization focused on improving consumer experiences Preferred Qualifications Prior experience supporting Humana or similar organizations Five or more years of professional proofreading experience Apex Systems is a world-class IT services company that serves thousands of clients across the globe. When you join Apex, you become part of a team that values innovation, collaboration, and continuous learning. We offer quality career resources, training, certifications, development opportunities, and a comprehensive benefits package. Our commitment to excellence is reflected in many awards, including ClearlyRated's Best of Staffing® in Talent Satisfaction in the United States and Great Place to Work® in the United Kingdom and Mexico. Apex uses a virtual recruiter as part of the application process. Apex Benefits Overview: Apex offers a range of supplemental benefits, including medical, dental, vision, life, disability, and other insurance plans that offer an optional layer of financial protection. We offer an ESPP (employee stock purchase program) and a 401K program which allows you to contribute typically within 30 days of starting, with a company match after 12 months of tenure. Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts. In terms of professional development, Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Apex has a dedicated customer service team for our Consultants that can address questions around benefits and other resources, as well as a certified Career Coach.