• You will be dedicated to a single client • You will be responsible for all site management and supervisory activities in the assigned oncology studies. • You will work with industry leaders and subject matter experts. • You will have the opportunity to mentor junior CRAs. • You will work with world-class technology. • You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.

• Perform site management activities to ensure compliance with the protocol, monitoring plan, ICH GCP, local regulatory requirements, and client SOPs. • Conduct site qualification, initiation, interim, and close-out visits, both on-site and remotely. • Partner with Clinical Trial Liaison (CTL) and other client functions to support site activation and deliverables. • Establish and maintain productive professional relationships with investigator site staff, ensuring effective communication and problem-solving throughout study conduct. • Perform drug accountability, reconciliation, and destruction, ensuring protocol compliance for storage and shipment requirements. • Prepare and maintain Oversight Monitoring Plan. • Conduct Oversight Monitoring Visits at sites, either independently or alongside CRO CRA. • Ensure site regulatory files are current and verify timely submission of study documentation, including safety reporting. • Identify and record protocol deviations, escalate non-compliance, and resolve study-related issues as necessary. • Maintain ongoing communication with site personnel, study teams, CTLs, Central Monitors, and CRO CRAs.

• 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.