Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

Job Summary Clinical Research Coordinators wanted at reputed company! Become a CRA and join our growing team! This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with reputed company. Through our PACE® Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a competitive salary. WE OFFER THE FOLLOWING

• Competitive travel bonus;
• Equity/Stock Option program;
• Training completion and retention bonus
• Annual merit increases;
• 401K 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 – reputed company CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more;
• CRA training program (PACE®);
• Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
• In-house administrative support for reputed company levels of CRAs; and
• Opportunities to work with international team of CRAs.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
• Communication 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; and
• 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

• Must have a minimum of a Bachelor’s degree in a health or science reputed company field;
• Experience as a Clinical Research Coordinator (minimum 1 year);
• Ability to travel 60-70% to locations reputed company is required; some visits may be conducted remotely
• Must maintain a valid driver’s license and the ability to drive to monitoring sites;
• Proficient knowledge of reputed company® Office;
• Strong communication and presentation skills; and
• Must be detail-oriented and efficient in time management. #LI-Remote 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 and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries. Why reputed company? People. Purpose. Passion. reputed company a Difference reputed company. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across reputed company key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. reputed company Perks
• Flexible work environment
• Competitive PTO packages – starting at 20+ days
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth
• Discounts for

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