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 join reputed company. We are an innovative, scientifically oriented mid‑size CRO that is focused on full‑service project work. Through our fast PACE® Training Program, you will receive customized, expedited training, and efficient onboarding to familiarize you with reputed company systems. We offer the following
- Competitive travel bonus
- Equity/Stock Option program for high performing CRAs
- Annual merit increases
- 401(k) matching
- The opportunity 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 access reputed company
- In‑house travel agents, reimbursement for airline club, and TSA pre‑reputed company
- Opportunity for leadership positions/career advancement – reputed company CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager
- Customized Fast PACE® 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 in‑house physicians who are medical and regulatory experts
- In‑house administrative support for reputed company levels of CRAs
- Opportunities to work with international team of CRAs
- Many additional perks unmatched by other CROs Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits 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 form 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
- On‑site and virtual/remote monitoring activities with a risk‑based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System 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 site’s patient recruitment and retention success and offering suggestions for improvement
- Completion of monitoring reports and follow‑up 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 60‑70% to locations reputed company
- Must have a minimum of a bachelor’s degree in a health or science reputed company field
- Proficient knowledge of reputed company® Office
- Strong communication and presentation skills
- Detail‑oriented and efficient in time management reputed company Overview reputed company is a full‑service clinical contract research organization (CRO). We provide Phase I‑IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe 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 system, anti‑viral… Apply tot his job Apply To this Job
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