Clinical Research Coordinator jobs in Greensboro, NC

What We Do 

Care 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 Are 

We 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 Overview 

The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This position has potential growth and advancement within the Care Access Research organization. 

What You'll Be Working On 

Duties include but not limited to: 

Ability to understand and follow institutional SOPs   

Participate in recruitment and pre-screening events (may be at another location) 

Assist with preparation of outreach materials  

Identify potential participants by reviewing medical records, study charts and subject database   

Assist with recruitment of new participants by conducting phone screenings  

Request medical records of potential and current research participants   

Schedule visits with participants, contact with reminders   

Obtain informed consent per Care Access Research SOP, under the direction of the CRC 

Complete visit procedures as required by protocol, under the direction of the CRC 

Collect, process and ship specimens as directed by protocol, under the direction of the CRC 

Record data legibly and enter in real time on paper or e-source documents  

Request study participant payments 

Update all applicable internal trackers and online recruitment systems 

Assist with query resolution   

Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc.   

Assist with maintaining all site logs  

Assist with inventory and ordering equipment and supplies  

Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. 

Maintain effective relationships with study participants and other care Access Research personnel. 

Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management. 

Communicate clearly verbally and in writing. 

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Physical and Travel Requirements 

This is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role. Overnight travel will be minimal (<10%). 

What You Bring 

Knowledge, Skills, and Abilities: 

Ability and willingness to work independently with minimal supervision 

Ability to learn to work in a fast-paced environment 

Excellent communication skills and a high degree of professionalism with all types of people 

Excellent organizational skills with strong attention to detail  

A working knowledge of medical and research terminology  

A working knowledge of federal regulations, Good Clinical Practices (GCP)  

Critical thinker and problem solver  

Friendly, outgoing personality with the ability to maintain a positive attitude under pressure 

Contribute to team and site goals 

Proficiency in Microsoft Office Suite  

High level of self-motivation and energy  

An optimistic, “can do” attitude 

Certifications/Licenses, Education, and Experience: 

A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist.   

Phlebotomy Experience and Proficiency Required 

Some Clinical Research experience preferred 

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 plan 

Diversity & Inclusion 

We 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.  

At Care Access, every day, we are advancing medical breakthroughs. We’re uniting standard patient care with cutting-edge treatments and research. Our work brings life-changing therapies to those in need and paves the way for newer and greater treatments to reach the world. We’re proud to advance these breakthroughs and work with the big players while engaging with the 

physicians and caring for patients. 

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. 

Care Access is currently unable to sponsor work visas.