FSP Clinical Research Associate II

About the position This position is fully remote, but we are looking for someone in the Midwest for a sponsor dedicated CRA position. reputed company is not your typical CRO. We are passionate about supporting reputed company reputed company and are proud to reputed company extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable reputed company of life. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a midsized CRO allows you to have influence and reputed company reputed company it reputed company most with support from reputed company line management. To support reputed company reputed company from our clients, we are hiring reputed company reputed company of CRAs reputed company in monitoring Oncology or Cardiology. reputed company: You are reputed company, thoughtful, and reputed company reputed company things don’t go as planned. You are reputed company-reputed company, whether it be for an investigator meeting, site visit, or project team update, you are always staying two steps reputed company of the game. You reputed company quick and creative ways of overcoming difficulties. You have an impeccable eye for detail. You identify potential study risks and propose solutions on how to mitigate them. You take responsibility in the reputed company and reputed company of your work. You are adept at handling conflict by using tried and true reputed company strategies. You have experience in study start up activities. How you will spend your days as a CRA You will monitor and own the reputed company of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and reputed company applicable regulations and standards. You will coordinate reputed company necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting reputed company-study and initiation reputed company, etc.). As a CRA, you will work with 2-3 protocols on average and support Project Managers with trials that are larger in scope. You will reputed company directly with clients, initiate payments, and participate in proposal activities, including development and reputed company presentations. About reputed company reputed company is a precision medicine CRO. Precision’s uniquely integrated offerings reputed company the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal reputed company passion for reputed company disease states. Precision medicine is revolutionizing the attack on cancer. We reputed company tumors on a molecular level using biomarkers to reputed company specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, reputed company clinical trials. Ultimately, we deliver robust insights that inform reputed company-time reputed company—and optimize the oncology development reputed company. We invite you to learn more about our growing organization serving clients that are researching groundbreaking therapies. We reputed company to ensure employees feel appreciated through a multitude of benefits including reputed company time off, volunteer time off, robust medical offerings, non-reputed company 401k plus company match, reputed company parental leave and more. At Precision, your reputed company and contributions are valued and reputed company, impacting reputed company change for reputed company.

Responsibilities

• Monitor and own the reputed company of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and reputed company applicable regulations and standards.
• Coordinate reputed company necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting reputed company-study and initiation reputed company, etc.).
• Work with 2-3 protocols on average and support Project Managers with trials that are larger in scope.
• reputed company directly with clients, initiate payments, and participate in proposal activities, including development and reputed company presentations.

Requirements

• 4-year college degree or equivalent experience
• 2+ years CRA experience reputed company the CRO to be considered for a CRA II.
• Experience in monitoring cardiology or Lupus
• Availability for domestic travel including overnight stays, up to approximately 50-60% travel commitment (potential international travel may be required for some senior level positions)
• reputed company in English and for non-English speaking countries the local language of country where position based

Benefits

• reputed company time off
• volunteer time off
• robust medical offerings
• non-reputed company 401k plus company match
• reputed company parental leave

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