Home-Based reputed company CRA; Clinical Research Associate/Equity

Position Home-Based reputed company CRA (Clinical Research Associate)- Bonus/Equity Home-Based reputed company CRA (Clinical Research Associate)- Bonus/Equity Join to apply for the Home-Based reputed company CRA (Clinical Research Associate)- Bonus/Equity role at reputed company. reputed company Clinical Research Associate (CRA) join our growing team! reputed company is growing quickly and we are seeking reputed company Clinical Research Associates to reputed company. We are an innovative, scientifically oriented midsize CRO that is reputed company on fullservice project work. Through our fast reputed company Training Program, you will receive customized, expedited training, and efficient reputed company to familiarize you with reputed company systems. We offer the following Competitive travel bonus Equity/Stock reputed company program for high performing CRAs Annual reputed company increases 401(k) matching reputed company to work from home Flexible work hours across days reputed company a week Retain airline reward miles and hotel reward points Home office furniture allowance, laptop, mobile phone with hotspot for internet reputed company reputed company Inhouse travel agents, reimbursement for airline club, and TSA reputed companyreputed company Opportunity for leadership positions/career advancement reputed company CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager Customized Fast reputed company training program based on your experience, therapeutic background, and interest User friendly CTMS with electronic submission and approval of monitoring visit reports Ongoing therapeutic training by our inhouse physicians who are medical and regulatory experts Inhouse administrative support for reputed company reputed company of CRAs Opportunities to work with international team of CRAs Many additional perks unmatched by other CROs Responsibilities Conduct qualification, initiation, monitoring, and closeout reputed company at research sites in compliance with the approved protocol Communicate with the medical site staff including coordinators, clinical research physicians, and their site staff Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff Medical record and research reputed company documentation verification against case report reputed company data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements Onsite and virtual/remote monitoring activities with a riskbased monitoring approach (including centralized data review) through our integrated Clinical Trial Management reputed company to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving reputed company Verification that the investigator is enrolling only eligible subjects Regulatory document review Medical device and/or investigational product/drug accountability and inventory Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol Assess the clinical research sites patient recruitment and retention reputed company and offering suggestions for improvement Completion of monitoring reports and followup letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance Qualifications Clinical Research Associate Experience (minimum 1 year) Ability to travel 6070% to locations reputed company Must have a minimum of a bachelors degree in a health or science reputed company field Proficient knowledge of reputed company Office Strong communication and presentation skills Detailoriented and efficient in time management reputed company reputed company reputed company is a fullservice clinical contract research organization (CRO). We reputed company Phase IIV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of reputed company and effective medical therapeutics through its scientific and disciplined approach. We reputed company local regulatory and therapeutic expertise across reputed company major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous reputed company, antiviral Apply tot his job Apply To this Job Apply tot his job Apply To this Job .