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Clinical Research Coordinator- Oncology- Macon, GA
Care AccessUnited Statesfull_timeVerifiedPosted 3 Sept 2024
About the role
What We DoCare Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.
Who We AreWe care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.
Position OverviewAs a Clinical Research Coordinator working at the Macon, GA site Monday – Friday you will be responsible for study coordination, including study start-up, patient recruitment, backup support, and other duties as required at the location.If you’ve never heard of anything like this before, that’s because it’s never been done before. The need for science has never been as great as it is today. That’s why we need you.
What You'll Be Working On:Serving as the primary contact to ensure appropriate communications, trial management, and meeting of timelinesCoordinating the operational aspects of a new and ongoing clinical trial at the siteWorking under the supervision of the Principal Investigator(s), while exercising excellent clinical judgment in patient monitoring and careMaintaining daily contact with the Principal Investigator(s) for recruitment activities, study start-up, and general daily communicationResponsible for the execution of trial protocol and ensuring all the sites team members are adequately trained and updated on the protocolPatient recruitment and pre-screeningMaintaining and submitting IRB communications and regulatory documentsTimely communications with internal teams, investigators, review boards, and study subjectsPreparing other study materials as requested by the Principal Investigator, such as: informed consent documents, case report forms, enrollment logs, and drug/device accountability logs
Physical and Travel Requirements:This is an on-site position with less than 10% travel requirements. Occasional planned travel may be required as part of the role. What You Bring Knowledge, Skills, and Abilities:● Good management and organizational skills, understanding of medical procedures● Exceptional interpersonal skills, the ability to work independently● Ability to lift a minimum of 50 pounds● Command of professional and Business English (written and spoken)
Certifications/Licenses, Education, and Experience: ● 3+ years of Oncology clinical trials experience as a Clinical Research Coordinator (CRC) including experience(s) with an Investigational New Drug (IND) or Investigational Product (IP) ● The position requires a least a High School Diploma or equivalency● Phlebotomy experience is a plus● Experience checking and documenting vitals and EKG (ECG) within the past year. ● Oncology experience is required Benefits (US Full-Time Employees Only)● PTO/vacation days, sick days, holidays. ● 100% paid medical, dental, and vision Insurance. 75% for dependents.● HSA plan● Short-term disability, long-term disability, and life Insurance. ● Culture of growth and equality● 401k retirement planDiversity & InclusionWe serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success. We do not discriminate based on race, sex, religion, color, national origin, gender identity, age, marital status, veteran status, or disability status. At Care Access, every day, we are advancing medical breakthroughs. We’re unitingstandard patient care with cutting-edge treatments and research. Our workbrings life-changing therapies to those in need and paves the way for newer andgreater treatments to reach the world
Who We AreWe care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.
Position OverviewAs a Clinical Research Coordinator working at the Macon, GA site Monday – Friday you will be responsible for study coordination, including study start-up, patient recruitment, backup support, and other duties as required at the location.If you’ve never heard of anything like this before, that’s because it’s never been done before. The need for science has never been as great as it is today. That’s why we need you.
What You'll Be Working On:Serving as the primary contact to ensure appropriate communications, trial management, and meeting of timelinesCoordinating the operational aspects of a new and ongoing clinical trial at the siteWorking under the supervision of the Principal Investigator(s), while exercising excellent clinical judgment in patient monitoring and careMaintaining daily contact with the Principal Investigator(s) for recruitment activities, study start-up, and general daily communicationResponsible for the execution of trial protocol and ensuring all the sites team members are adequately trained and updated on the protocolPatient recruitment and pre-screeningMaintaining and submitting IRB communications and regulatory documentsTimely communications with internal teams, investigators, review boards, and study subjectsPreparing other study materials as requested by the Principal Investigator, such as: informed consent documents, case report forms, enrollment logs, and drug/device accountability logs
Physical and Travel Requirements:This is an on-site position with less than 10% travel requirements. Occasional planned travel may be required as part of the role. What You Bring Knowledge, Skills, and Abilities:● Good management and organizational skills, understanding of medical procedures● Exceptional interpersonal skills, the ability to work independently● Ability to lift a minimum of 50 pounds● Command of professional and Business English (written and spoken)
Certifications/Licenses, Education, and Experience: ● 3+ years of Oncology clinical trials experience as a Clinical Research Coordinator (CRC) including experience(s) with an Investigational New Drug (IND) or Investigational Product (IP) ● The position requires a least a High School Diploma or equivalency● Phlebotomy experience is a plus● Experience checking and documenting vitals and EKG (ECG) within the past year. ● Oncology experience is required Benefits (US Full-Time Employees Only)● PTO/vacation days, sick days, holidays. ● 100% paid medical, dental, and vision Insurance. 75% for dependents.● HSA plan● Short-term disability, long-term disability, and life Insurance. ● Culture of growth and equality● 401k retirement planDiversity & InclusionWe serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success. We do not discriminate based on race, sex, religion, color, national origin, gender identity, age, marital status, veteran status, or disability status. At Care Access, every day, we are advancing medical breakthroughs. We’re unitingstandard patient care with cutting-edge treatments and research. Our workbrings life-changing therapies to those in need and paves the way for newer andgreater treatments to reach the world
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