{"id":726176,"url":"https://alion.io/job/clinchoice-senior-clinical-research-associate","title":"Senior Clinical Research Associate","company":{"id":672996,"name":"ClinChoice","domain":"clinchoice.com","url":"https://alion.io/company/clinchoice","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Greenhouse","truth_index":{"grade":"B","score":78,"open_postings":13,"ghost_share":0,"stale_share":0.846,"repost_share":0.077,"time_to_fill_p50_days":39,"computed_at":"2026-11-02T06:13:15Z"}},"role":"Biotech","role_family":"Biotech","seniority":"senior","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"posting_text","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["United States"],"countries":["US"],"hiring_countries":["US"],"hiring_countries_total":1,"salary":null,"salary_estimate":{"min_usd":90000,"max_usd":183000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":154},"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false},{"name":"Microsoft Office","optional":false},{"name":"Outlook","optional":false}],"status":"live","first_seen_at":"2026-08-11T07:17:31Z","employer_posted_date":"2026-10-26","last_verified_at":"2026-11-02T11:12:00Z","board_verified":true,"closed_at":null,"days_open":83,"trust":{"level":"ok","repost_count":2,"flags":["repost"],"days_open":82},"description":"ClinChoice is a global, full-service CRO providing clinical research services to pharmaceutical, biotechnology, medical device and consumer health companies. We are currently seeking an experienced Senior Clinical Research Associate (Senior CRA) to join our in-house team.\nAs a Senior CRA, you will manage 2-3 clinical trials and be responsible for site management activities, including study start-up, site monitoring, and closeout. You'll conduct both on-site and remote monitoring while supporting a variety of studies across a diverse client portfolio, from emerging biotech companies to large pharmaceutical organizations.\nThis is a permanent, fully remote position. Candidates must be willing and able to travel to investigative sites as needed.\nCandidates must have experience monitoring oncology and other complex clinical trials, as well as previous experience working for a CRO. A strong understanding of GCP, ICH guidelines, and clinical trial operations is also required.\nJoin our team: you can be part of making a difference in people’s lives and experience a fulfilling and rewarding career!\nThis is a remote role, ideal locations areWest Coast, Northeast and/or Florida. \n Main Job Tasks and Responsibilities:\nKeep professionally abreast of all scientific, regulatory and operational aspects relevant to the clinical projects assigned.\nAssist in the selection of sites, site evaluation visits, initiation visits and ensure follow-up by obtaining pre-study documentation to ensure good start-up of the investigation sites.\nMay act as Feasibility Associate.\nTrain site staff in all study procedures.\nConduct periodic monitoring visits, including completion of monitoring visit report. Review at each visit the accuracy, legibility, completeness and quality of the Case Report Forms (CRF).\nConduct source data verification and in-house review of clinical data and ensure timely resolution of data queries to guarantee reliable clinical data.\nManage the investigational products (storage, inventory, dispensing records, packaging and labelling) and the trial material (Investigator Study File (ISF), CRF, questionnaires, diaries, etc.) to ensure timely and correct supply to the site.\nCooperate with the site staff to ensure proper reporting from the site for safety issues (AEs, SAEs, SUSARs, etc.) and their follow-up, guaranteeing timely and appropriate handling of safety issues.\nConduct and report study termination and related activities (e.g. archiving) guaranteeing smooth completion of the project.\nAct as the main contact person for the site to ensure close follow up.\nProvide general support to the Clinical Research Division on quality control of clinical data.\nAddress appropriate team members about any issues that can jeopardise the conduct of the clinical projects assigned in a timely manner.\nReport to the Head of department on all activities performed during the study and send all relevant documents according to the timelines and the requirements agreed for each single clinical trial.\nDevelop training material and give training in collaboration with the Training & Qualification Management Unit.\nMay assist with contract negotiation with sites on study budget after appropriate training.\nAssist with the preparation of the study, including CRF design/development, write CRF instructions and organise the study files and documents to ensure good start-up of the investigation sites.\nMay support the submission process in the project including submission requirements, timelines, informed consent development, etc..\nGuide and supervise Clinical Research Associate I (CRA I) to coach and train them on the job.\n Education, Experience and Skills:\nUniversity Degree in scientific, medical or paramedical disciplines. Bachelor's Degree or equivalent University Degree in scientific and/or medical or paramedical disciplines; Nursing degree or relevant degree or background preferred. In some cases, an equivalency, consisting of a combination of appropriate education, training and or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.\n\nPrevious experience working for a CRO is required.\nAt least eight (8) years of clinical research experience, including proven experience as a Clinical Research Associate (CRA) performing on-site monitoring activities.\nExperience with oncology, respiratory and complex trials is required. \nStrong knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory requirements.\nFluent in English and local language(s).\nProficiency in Microsoft Office (e.g., Word, Excel, Outlook).\nWillingness to travel\nThe Application Process\nOnce you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.\nWho will you be working for?\nAbout ClinChoice \nClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. \nOur Company Ethos\nOur mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.\nClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.\n Key words: Clinical Research Associate, CRA, Permanent, CRO, Contract Research Organization, Outsourced, Outsourcing, Oncology, Monitoring, Early Phase Oncology Trials, Senior CRA, Oncology Clinical Trials, CAR T, Investigative Site Monitoring, On-site Monitoring, Remote Monitoring, 1.0 FTE, Travel, GCP (Good Clinical Practice), ICH Guidelines, FDA Regulations, Regulatory Compliance, Clinical Trial Operations, Source Data Verification (SDV), Case Report Forms (CRFs), Data Query Resolution, Safety Reporting (AE, SAE, SUSAR), Investigational Product (IP) Management, Site Initiation Visits (SIV), Site Selection Visits (SSV), Close-Out Visits (COV), Feasibility Assessment, Site Management, Study Start-Up, Clinical Data Quality Control, Monitoring Visit Reports, Investigator Study File (ISF), Trial Master File (TMF), Clinical Study Documentation, Site Training, Study Budget Negotiation, Informed Consent Development, Submission Support, 8+ Years CRA Experience, Advanced Oncology Experience, Phase I Oncology Monitoring, Early-Phase Oncology Trials, CRO Experience, U.S.-Based CRA\n#LI-VH #LI-Remote #Senior Clinical Research Associate # 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