In House Clinical Reseach Associate

🔗Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.Job Description SummaryJob DescriptionTHE IN-HOUSE CLINICAL RESEARCH ASSOCIATE (CRA) ROLEThe Sr. In-house CRA is an important member of the Alira Health Clinical team. Sr. In-house CRAs manage and support clinical sites from site approval through close-out. Sr. In-house CRAs work closely with field CRAs and Clinical Project Managers to ensure the integrity of the trial data without the need for frequent travel.ESSENTIAL JOB FUNCTIONSDevelops study documents and tools, including Informed Consent Form (ICF) templates (for both local and central IRBs), Investigator Site File (ISF) contents, etc.Supports sites in obtaining IRB approval, developing submission materials, and creating sitespecific ICFsResponds to sites’ regulatory board requests for protocol and ICF clarification as neededEnsures all required site regulatory documents and approvals are in place prior to investigational product shipmentEnsures all regulatory documents are collected and filed appropriately at both the site and in the Trial Master File (TMF); conducts routine file reviewsAnalyzes site performance problems (protocol adherence) and identifies solutions; provides ongoing training for study sitesMaintains regular communication with study sites to ensure protocol/GCP compliance, assesses subject accrual rates, and responds to sponsor requestsConducts remote review of data entered on electronic Case Report Forms (eCRFs) as neededWorks closely with field CRAs and data management to resolve queries on discrepant dataAssists with efforts to recruit investigative sites to participate in clinical studiesComplies with ICH GCP guidelines, FDA regulations, and company SOPsParticipates in internal, client/sponsor, scientific, and other meetings as requiredManages and resolves conflicting priorities to deliver on commitmentsPerforms additional duties as assignedPREPARATION, KNOWLEDGE, SKILLS & ABILITIESBS/BA from an undergraduate program or equivalent experienceAt least 7 years of experience in clinical researchProven ability to be careful, thorough, and detail-orientedStrong organizational skills and the ability to multi-task and work effectively in a fast-paced environmentStrong analytical, negotiation, meeting management, cross-functional team, and leadership skillsSelf-starter who thrives in a collaborative, yet less structured team environmentAbility to problem-solve unstructured or ambiguous challengesStrong command of English, both written and verbalExcellent communication and interpersonal skills with customer service orientationProficient with MS Office Suite, particularly Word and ExcelPermanent authorization to work in the U.S.WORKING CONDITIONS/PHYSICAL DEMANDSNormal office working conditions including frequent sitting, standing, bending, twisting and computer monitor use. Occasional lifting of weight up to 30 lbs.Compensation: $85,000 - 100,000 commensurate with experienceLanguagesEnglishEducationBachelor of Science (BS)Contract TypeRegular

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