{"id":1756853,"url":"https://alion.io/job/evolution-research-group-cro-project-manager","title":"CRO-Project Manager","company":{"id":3876300,"name":"Evolution Research Group","domain":"ergclinical.com","url":"https://alion.io/company/evolution-research-group","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"ADP","truth_index":{"grade":"B","score":75,"open_postings":11,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-10-10T05:45:15Z"}},"role":"Management","role_family":"Management","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"inferred","locations":[],"countries":[],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Microsoft Office","optional":true}],"status":"live","first_seen_at":"2026-09-08T22:39:00Z","employer_posted_date":"2026-09-08","last_verified_at":"2026-10-10T20:11:51Z","board_verified":true,"closed_at":null,"days_open":32,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":32},"description":"Job Title: Project Manager\nLocation: Remote\nJob Description:\nThe Project Manager is a proven leader in clinical program management in the clinical research industry, and manages, executes, and reports on clinical study operations. This position provides leadership and support to members of the multidisciplinary project team, internally and externally. Responsibilities encompass the overall management of a project including budgeting, timeline adherence, internal and external communications, and project deliverables. Under limited to no supervision, act as the liaison between the sponsor, team members, and sites while managing projects to ensure quality service. This position will be part of the Clinical Operations Team, which is responsible for planning, executing, managing, and closing projects associated with the company clinical study plans.\nEssential Duties and Responsibilities:\nAssume primary accountability for assigned clinical research projects and ensure compliance with applicable regulations, guidelines, and corporate policies for study activities. \nManage and execute the overall project scope, budget, and timelines. Identify project success factors for analysis, reporting, and tracking. \nManage resources and timelines associated with all study start-up and implementation activities, including CRO/investigator agreements, and contractual agreements. \nLead the development of study specific protocols, consent forms, and other trial related materials as required. \nEnsure the appropriate development of study documents including, but not limited to, study plans, case report form instructions, site selection materials, investigator updates, and other project-specific documents required for the conduct of assigned studies. \nParticipate in the review of clinical data for analysis. \nEnsure that all project tasks meet client expectations and are completed in accordance with the contract, trial protocol, and Standard Operating Procedures (SOPs). \nServe as a liaison between clients and internal team to ensure project specific information and ongoing updates are proactively communicated. \nPlan for and manage all materials to support the appropriate execution of the clinical projects, including but not limited to distribution of documents, forms, supplies, equipment, and investigational device. Monitor adherence to project contract and budget.\nCoordinate with clinical, marketing, and operations management to identify goals and scope of clinical study projects. Ensure operational and regulatory integrity of assigned studies and participate in FDA or other regulatory authority inspections, as needed. \nSupport the management and oversight of clinical study related vendors. Review site monitoring reports ensuring finalization as required by SOP and/or client contractual requirements.\nProvide therapeutic training and guidance to clinical team. \nEnhance department and organization reputation by participating in departmental or corporate initiatives.\nUpdate job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. \nAttending off-site meetings and conferences, as needed.\nPerform other miscellaneous related duties, as required.\nEducation and/or Experience:\nBachelor’s degree or equivalent education/degree in life science/healthcare is required accompanied by 5 years of working within clinical project management at a local medical organization, investigational site, pharmaceutical company, CRO, or clinical fellowship program. \nCRO experience is highly desirable. \nExperience qualifying & managing external vendors. \nExperience leading project operational teams through the start-up, study conduct, data management, and report writing of clinical studies. \nExperience writing, reviewing, and editing protocols and clinical study reports as well as working knowledge of the FDA submission process.\nSkills and Abilities:\nAbility to facilitate a teamwork philosophy with a positive attitude. \nExtensive organizing and coordinating skills, teaching and facilitation skills, ability to assess training needs and objectives. \nExtensive experience overseeing and coordinating the work of others. \nAbility to work effectively and efficiently handling multiple tasks simultaneously. \nAbility to exercise judgment and determine appropriate action to a variety of problems of varying complexity. \nAbility to manage multiple deadlines. \nMust have a ‘can-do’ attitude and a strong desire to take ownership of many different projects. \nStrong computer skills, including Microsoft 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