Clinical Trial Associate, APAC (Contract)

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.PositionAs a Clinical Trials Associate, APAC in Oncology, you will play a crucial role in supporting the planning, coordination, and execution of Phase I-III insourced global clinical studies within the oncology portfolio. Operating in a dynamic and collaborative environment, you will provide essential support for the execution of clinical trials, contributing to the development of groundbreaking therapies with the potential to transform patient lives.This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City (NJ) or Millbrae (CA) offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.This position requires fluency in Mandarin, Cantonese, Japanese, or Korean candidates without this qualification will not be considered due to the nature of interacting with locally based trial sites in Asia. About You You are passionate about playing a key role in supporting the planning, coordination, and execution of clinical trials within the oncology portfolio. You have strong communication skills and a passion for advancing care to patients.What You'll DoAssist in the preparation and maintenance of essential study documents, including study protocols, informed consent forms, case report forms (CRFs), and other trial-related materialsCollaborate with cross-functional teams to ensure accurate and timely completion of study start-up activities, such as site selection, feasibility assessments, and ethics committee submissionsSupport the organization and conduct of investigator meetings, study initiation visits, and other trial-related meetingsCoordinate and track the distribution, collection, and reconciliation of trial supplies, investigational products, and study related materialsAssist in the review and resolution of data queries, ensuring data accuracy and completeness within electronic data capture (EDC) systemsIn collaboration with TMF Operations team, maintain trial master files (TMFs) and study documentation in accordance with regulatory requirements and internal SOPsFacilitate effective communication among study team members, investigators, and study site personnel through regular correspondence and timely dissemination of study-related informationSupport the monitoring and tracking of study progress, including patient recruitment and enrollment, to ensure adherence to study timelines and milestonesIn collaboration with other Clinical Operations groups (Site Engagement and Monitoring Excellence) assist, as necessary, in the preparation and coordination of site monitoring visits, ensuring compliance with monitoring plans and resolution of site-related issuesStay updated with relevant regulations, guidelines, and industry best practices pertaining to oncology clinical trials, ensuring compliance, and implementing necessary changes as requiredQualificationsAn Advanced Degree without experience or Bachelor's degree with 2 years of experience in a relevant field (e.g., life sciences, healthcare, or related discipline)Ability to communicate in multiple languages required.Previous experience working as a Clinical Trials Associate, Study Coordinator, or in a similar role within the pharmaceutical, biotechnology, or CRO industry is preferredKnowledge of clinical trial regulations, guidelines, and best practices, including ICH-GCP and FDA requirementsStrong organizational skills and attention to detail, with the ability to manage multiple tasks and prioritize workload effectivelyProficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systemsExcellent written and verbal communication skills, with the ability to effectively interact with study team members and internal / external stakeholdersAbility to work independently as well as collaboratively in a team-oriented environmentProficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Project)Adaptability and willingness to learn and embrace new technologies, processes, and industry trendsThe expected hourly range for this role is $50/hour to $54.80/hour depending on skills, competency, and the market demand for your expertise. This is a contract role, expected to last approximately 12 months, with an anticipated workload of 40 hours per week. Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.

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