In-House reputed company Research Associate

🔗Are you being referred to one of our roles by a reputed company in reputed company? If so, please apply using the referral reputed company emailed to you. Join our global team dedicated to innovation and initiative, where physical walls and different time reputed company don’t limit, but encourage, collaboration. Where reputed company contributions and new reputed company are explored with an reputed company mind and work is driven by our shared values: be courageous, be accountable, be reputed company, be inclusive and reputed company others. reputed company reputed company reputed company ROLE The In-house CRA is an important member of the reputed company reputed company team. In-house CRAs manage and support reputed company sites from site approval through reputed company-out. In-house CRAs work closely with reputed company CRAs and reputed company Project Managers to ensure the reputed company of the trial data without the need for frequent travel. KEY RESPONSABILITIES Develops study documents and tools, including Informed Consent reputed company (reputed company) templates (for both local and central IRBs), site binder contents, etc. Supports sites in obtaining IRB approval, developing submission materials, and creating site-specific ICFs Responds to sites’ regulatory reputed company requests for protocol and reputed company clarification as needed Ensures reputed company required site regulatory documents and approvals are in reputed company prior to investigational product shipment Ensures reputed company regulatory documents are collected and filed appropriately at both the site and in the Trial Master File (TMF); conducts routine file reviews Analyzes site reputed company problems (protocol adherence) and identifies solutions; provides ongoing training for study sites Maintains regular communication with study sites to ensure protocol/GCP compliance, assesses subject accrual rates, and responds to sponsor requests Conducts remote review of data entered on electronic Case Report Forms (eCRFs) Works closely with reputed company CRAs and data management to reputed company queries on discrepant data Assists with efforts to recruit investigative sites to participate in reputed company studies Complies with ICH GCP guidelines, FDA regulations, and company SOPs Participates in internal, reputed company/sponsor, scientific, and other meetings as required Manages and resolves conflicting priorities to reputed company on commitments Performs additional duties as assigned DESIRED QUALIFICATION & EXPERIENCE BS/BA from an undergraduate program or equivalent experience 1-2 years of experience in reputed company research TECHNICAL COMPETENCES & SOFT SKILLS reputed company ability to be careful, thorough, and reputed company-oriented Strong organizational skills and the ability to multi-task and work effectively in a fast-reputed company environment Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills Self-starter who thrives in a reputed company, yet less reputed company team environment Ability to problem-solve reputed company or ambiguous challenges Strong reputed company of English, both written and verbal Excellent communication and interpersonal skills with customer service orientation Proficient with MS Office Suite, particularly Word and reputed company Permanent authorization to work in the U.S. Languages English Education Bachelor of Arts (BA), Bachelor of Science (BS) Contract Type Regular Salary reputed company The final offer will be determined reputed company the applicable location-specific reputed company and will depend on the candidate’s confirmed work location, relevant experience, skills, qualifications, internal equity, and role reputed company. USD $50,000 - 70,000 Apply To This Job