• Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies • Serve as the main CTI contact for assigned study sites • Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in the Monitoring Plan while adhering to all applicable regulatory requirements, SOPs, and ICH GCP • Assist with study start-up activities, including feasibility, pre-study activities, and site selection • Collect, review, and track essential/regulatory documents • Participate in and complete all general and study-specific training as required • Participate in investigator, client, and project team meetings • Create and implement subject enrollment strategies for assigned study sites • Ensure proper storage, dispensation, and accountability of all Investigational Product (IP) and trial-related materials • Perform site management activities and provide ongoing updates of site status to the Clinical Project Manager • Conduct remote monitoring and complete related activities in accordance with study-specific Monitoring Plan • Utilize systems and reports to track subject status, subject case report form (CRF) retrieval/source document review (SDV), regulatory documents, and IP • Assist with project-specific activities as a member of the Project Team • May support in the development of CRFs and other study-related documents (subject worksheets, Monitoring Plan, etc.) • May support in the translation, customization, and review of Patient Information sheet and Informed Consent, protocol synopsis, and other study-applicable documents as per required procedures • Where applicable, provide support to the Regulatory Affairs Study Start-up Team in the preparation or revision of documentation for submission to Ethics Committee(s), Institutions' Ethics Committees, Regulatory Authorities, Competent Authorities or Institutions Administration Boards, and follow up on the evaluation process until approval is available. • Provide regular updates to the Sponsor/ Client • Assist in preparing and coordinating Investigator and client meetings, and attend meetings as necessary • Liaise with Clinical Data Management for data cleaning activities • Identify site issues and implement corrective actions or escalate as appropriate • Manage ISF and TMF for all assigned study sites in accordance with SOPs or study-specific Monitoring Plans • Where applicable, support in contract negotiation with study sites, Investigator payments, and tracking of site payments

Role Description Chainlink Labs is seeking Research Interns to support its mission of building the world’s most secure and flexible decentralized oracle technologies. Research Engineers will work directly with top domain experts in applied cryptography, mechanism design (cryptoeconomics), distributed systems, and other disciplines to identify and solve key research challenges and build production solutions that keep Chainlink at the forefront of oracle system deployment and fuel the success of the smart contract ecosystem. - Working with Chainlink core engineering to identify short- and long-term research challenges critical to the company’s success and to transition innovations from Chainlink Labs into production. - Working with research scientists and technical advisors to study, invent, and build cutting-edge oracle technologies for the benefit of the company and community. - Staying abreast of the evolution of relevant technology ecosystems and participating in relevant technical communities for more effective application development and to guide research toward practical and impactful work. Qualifications - B.S. in computer science or equivalent professional experience along with coursework in algorithms and data structures and discrete math. - Familiarity with academic process and ability to engage with existing literature on relevant research topics, e.g. by performing literature searches and comprehending papers in a wider context. - Professional software development experience is required. Requirements - Advanced computer science or related degree, coursework in applied and theoretical cryptography, mechanism design, distributed systems, or related fields. - Familiarity with Go or Rust. - Broad knowledge of blockchain technologies and familiarity specifically with smart contracts. Benefits - All roles with Chainlink Labs are global and remote-based. - We carefully review all applications and aim to provide a response to every candidate within two weeks after the job posting closes. - The closing date is listed on the job advert, so we encourage you to take the time to thoughtfully prepare your application. - We want to fully consider your experience and skills, and you will hear from us regarding the status of your application shortly after the closing date. Commitment to Equal Opportunity Chainlink Labs is an equal opportunity employer. All qualified applicants will receive equal consideration for employment in compliance with applicable laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us via this form. Global Data Privacy Notice for Job Candidates and Applicants Information collected and processed as part of your Chainlink Labs Careers profile, and any job applications you choose to submit, is subject to our Recruiting Privacy Policy. By submitting your application, you are agreeing to our use and processing of your data as required.

• Research and test AI tools in creator communities • Build playbooks and best-practice guides for editors and producers • Partner with editors and producers to find AI efficiencies in productions • Support the edit team by contributing real work when needed • Collaborate with legal, engineering, and product teams on evaluation and decisions

Role Description In Accenture, within the Strategy & Consulting – Global Network area, we work with leading global clients to design and implement strategies that drive transformation and sustainable growth. As part of our team, you will collaborate on projects that combine innovation, deep analysis, and strategic execution, helping organizations tackle their most complex challenges. HOW WILL YOUR EVERYDAY BE? 💥 - Partner with global Life Sciences companies to drive R&D transformation, optimize clinical and regulatory processes, and enable digital innovation across the drug development lifecycle. - Support R&D strategy and transformation programs while designing and optimizing clinical, regulatory, and lab processes. - Enable technology implementations across R&D platforms. - Contribute to proposals and business development initiatives. - Develop thought leadership and reusable assets for the Life Sciences R&D practice. Qualifications - Bachelor’s degree (MBA/Postgraduate degree preferred). - Careers that strongly fit this role include Biotechnology, Pharmacy, Biology, Biochemistry, Chemistry, Biomedical Engineering, Clinical Research, and Bioinformatics. - 1–3+ years of experience in Life Sciences and/or consulting for Analysts, or 3-10+ years of experience for Consultants. - Advanced English is mandatory. Requirements - Experience in at least two R&D areas such as Clinical Operations / Clinical Development, Pharmacovigilance, Regulatory Affairs, Lab Informatics (R&D/QC Labs/LIMS, ELN), Quality Management Systems, or AI in Life Sciences. - Knowledge of R&D platforms such as Veeva Clinical Suite, Veeva RIM, CTMS, LIMS, ARGUS, ELN, Medidata RAVE is highly valued. - Experience in R&D operating model design and process transformation (desirable). - Exposure to digital clinical trials or automation initiatives (desirable). Benefits - PedidosYa credits - Swiss Medical health insurance – fully covered for you and your immediate family - Connectivity and electricity reimbursement - VIP Gym Pass – 100% covered - Days off starting from your first year of service - Flexible holidays - Flexible work shifts - Bonus for higher education certifications - Day off on your birthday - Performance bonuses - Extended maternity & paternity leave - Daycare reimbursement - And many more!