{"id":1996978,"url":"https://alion.io/job/novotech-cro-clinical-research-associate-flex-3","title":"Clinical Research Associate Flex","company":{"id":2899574,"name":"Novotech","domain":"novotech-cro.com","url":"https://alion.io/company/novotech-cro","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Oracle","truth_index":{"grade":"B","score":76,"open_postings":4,"ghost_share":0,"stale_share":0.75,"repost_share":0,"time_to_fill_p50_days":68,"computed_at":"2026-10-25T05:49:26Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"middle","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Beijing, China","Shanghai, China","Zhengzhou, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":27000,"max_usd":64000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":760},"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false}],"status":"live","first_seen_at":"2026-09-02T03:34:13Z","employer_posted_date":"2026-10-09","last_verified_at":"2026-10-25T04:24:15Z","board_verified":true,"closed_at":null,"days_open":53,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":53},"description":"Responsibilities\nPerforming site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations.\nSupporting the development of a subject recruitment plan.\nEstablishing regular lines of communication plus administering protocol and related study training to assigned sites.\nEvaluating the quality and integrity of site practices - escalating quality issues as appropriate.\nManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.\nAssist of country and/or site start up activities, including but not limit to country/site ICF development, preparation of IRB submission package, site contract and budget negotiation, and regulatory documents collection.\nPerform the tasks assigned by line manager.\nExperience and Qualifications\nBS (Bachelor of Science) degree or equivalence experience. Advanced degree is a plus.\nAt least 2.5 year experience in clinical research environment.\nGood command of written and spoken in English, good organization and communication skills.\nHigh attention to detail and accuracy.\nNovotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.\nOur team members are passionate about what we do, but we understand work is only one of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.\nWe are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.\nWe are a Circle Back Initiative Employer and commit to respond to every application. 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