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Clinical Research Assistant -Chicago, IL

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. 

 

Employment Statement

Care Access complies with all employment laws and regulations with respect to its employment practices, terms and conditions of employment, and pay equity and wages. Care Access does not engage in any unfair or forced labor practice and does not tolerate, under any circumstances, the use of any form of forced or involuntary labor, child labor, or human trafficking. This extends to suppliers, partners, or other third parties with whom Care Access does business. Care Access values and promotes the protection of human rights everywhere.


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CEO of Care Access
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Average salary estimate

$57500 / YEARLY (est.)
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$50000K
$65000K

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What You Should Know About Clinical Research Assistant -Chicago, IL, Care Access

Are you ready to launch your career in clinical research? Care Access, based in Chicago, IL, is looking for a passionate Clinical Research Assistant to join our team! Imagine being part of a company that's revolutionizing access to clinical trials, allowing us to accelerate the approval and delivery of life-saving therapies. In this entry-level position, you'll dive deep into the Care Access Research process while gaining valuable skills that can pave the way to becoming a Clinical Research Coordinator. Your responsibilities will be diverse and engaging – from participating in participant recruitment and pre-screening events to managing medical records and study charts. You'll assist with obtaining informed consent and ensure all procedures follow established protocols. We are looking for someone with excellent communication skills, a knack for organization, and a positive, can-do attitude. As an integral part of our mission to enhance clinical trial access, you will also maintain effective relationships with study participants and internal teams. With opportunities to grow within Care Access, your journey in the world of clinical research could lead to impactful contributions that save lives. If you're motivated, eager to learn, and excited about the challenge, we can't wait to meet you and discuss how you can make a difference in healthcare!

Frequently Asked Questions (FAQs) for Clinical Research Assistant -Chicago, IL Role at Care Access
What qualifications are needed to be a Clinical Research Assistant at Care Access?

To be a Clinical Research Assistant at Care Access, candidates should have a minimum of one year of recent experience in roles such as Medical Assistant, EMT, LPN, Clinical Research Assistant, or Phlebotomist, along with proficiency in phlebotomy. Familiarity with medical and research terminology is essential, as well as knowledge of federal regulations and Good Clinical Practices (GCP). Ideal candidates are energetic, detail-oriented, and possess excellent communication skills.

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What are the main responsibilities of the Clinical Research Assistant role at Care Access?

In the Clinical Research Assistant role at Care Access, you'll be responsible for recruiting and pre-screening participants for clinical trials, preparing outreach materials, and ensuring compliance with institutional SOPs. Additionally, you'll handle data entry, maintain study logs, and assist with administrative tasks. A major part of your job will involve interacting positively with participants, obtaining informed consent, and working alongside the Clinical Research Coordinator to execute visit procedures.

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What types of skills are important for success as a Clinical Research Assistant at Care Access?

Success as a Clinical Research Assistant at Care Access hinges on strong organizational skills, attention to detail, and the ability to communicate effectively with various stakeholders. A critical thinker and friendly personality will help you maintain professional relationships with participants and colleagues. Additionally, being able to work independently while navigating the fast-paced research environment is crucial.

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Can you describe the work environment for the Clinical Research Assistant at Care Access?

The work environment for a Clinical Research Assistant at Care Access is dynamic and collaborative. You will primarily work on-site in the Chicago area, often engaging with study participants and research teams. The role may require occasional travel for recruitment events, but overnight travel is minimal. This position fosters a culture of growth and equality, where diverse ideas and teamwork are encouraged to advance medical breakthroughs.

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What growth opportunities exist for a Clinical Research Assistant at Care Access?

Care Access offers significant growth opportunities for Clinical Research Assistants. By gaining hands-on experience and mastering the essential skills required for the role, you can advance to positions such as Clinical Research Coordinator. The company values internal promotions and professional development, providing a supportive environment for your career advancement within the Care Access Research organization.

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Common Interview Questions for Clinical Research Assistant -Chicago, IL
What motivated you to apply for the Clinical Research Assistant position at Care Access?

When answering this question, highlight your passion for clinical research and how Care Access's mission resonates with your values. Discuss your desire to contribute to life-saving therapies and how the company's innovative approach to clinical trials aligns with your career goals.

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How do you prioritize tasks and manage your time effectively in a fast-paced environment?

You can demonstrate your organizational skills by discussing methods you use, such as creating to-do lists, setting deadlines, and assessing task urgency. Share examples from previous experiences where you successfully managed multiple responsibilities.

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Describe a challenging situation you faced in a previous role and how you resolved it.

Use the STAR (Situation, Task, Action, Result) method to structure your response. Choose a relevant example, explain the challenge, and illustrate the steps you took to resolve it while emphasizing your problem-solving skills.

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What is your experience with participant recruitment and how would you handle difficult conversations?

Share any previous experience you have in participant recruitment and create a strategy for approaching difficult conversations. Emphasize the importance of compassion and professionalism in your interactions, highlighting your communication skills.

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How would you ensure compliance with federal regulations and Good Clinical Practices?

You can answer this question by discussing your understanding of federal regulations and GCP guidelines, as well as your commitment to meticulous task execution. Mention any relevant training or certifications to reinforce your knowledge.

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Can you explain the role of data management in clinical research?

Discuss how data management is critical in clinical research for ensuring that data collected is accurate, reliable, and timely. Explain your familiarity with data entry processes and your attention to detail in maintaining accurate records.

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What qualities do you believe are essential for a Clinical Research Assistant?

Consider emphasizing communication, organization, attention to detail, and the ability to work in a team. Highlight that flexibility and a positive attitude are also vital as they contribute to a harmonious workplace environment.

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Describe your understanding of the informed consent process in clinical trials.

Include the key elements of informed consent—ensuring participants fully understand the study, its risks, and benefits. Discuss your ability to communicate these elements clearly and ethically, which is vital for building trust with participants.

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How do you handle feedback and criticism in the workplace?

Share how you view feedback as an opportunity for growth. Provide examples of how you have responded positively to constructive criticism in the past and the steps you took to apply the feedback effectively.

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What do you hope to gain from your experience as a Clinical Research Assistant at Care Access?

Express your eagerness to learn and grow within the clinical research field. Discuss specific skills or experiences you hope to acquire during your time at Care Access, emphasizing your commitment to the organization’s mission.

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Our goal is to engage every healthcare professional in clinical research and to make clinical trials a care option for every patient

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EMPLOYMENT TYPE
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DATE POSTED
March 7, 2025

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