Central Study Coordinator - Retention

About Care Access

Care Access is working to make the future of health better for all.  With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care.  We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need,  and contribute to the medical breakthroughs of tomorrow.

With programs like  Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and  Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit  www.CareAccess.com .

How This Role Makes a Difference

The Central Study Coordinator – Retention (CSC-R) position combines clinical research and patient education skills into a singular role that delivers a strong customer experience for participants of patient programs, primarily the Future of Medicine program. The CSC-R acts as a virtual partner to individuals participating in the program and who are interested in learning more about clinical research. The CSC-R is accountable for ensuring the participants of the Future of Medicine are properly educated, retained, and considered for study participation. CSC-Rs do this several ways including but not limited to sharing and explaining lab results, conducting virtual consenting appointments, and pre-screening participants for specific studies. This role is expected to coordinate daily work independently using patient centric practices and a quality-first approach. This is a mid-level individual contributor role with the expectation that the CSC-R has strong working knowledge of and experience in the clinical research industry and excellent interpersonal skills.  

How You'll Make An Impact

Lab Result Return (Patient Education)

Educate participants on lab results received through a Future of Medicine screening event and ensure the results are understood

Educate and prepare participants on potential study opportunities using the provided educational materials and tools

Assess if a patient is understanding their results or if more support is needed, including a potential discussion with a licensed professional in the provider team

Use good judgment and time management in providing the time and care needed by each Future of Medicine member to understand their results, potential studies, and address any questions they have, while also working through daily quotas of member calls, all while maintaining a patient-first mindset

Study Matching

Build strong rapport with participants in a virtual environment to help ensure a positive experience for everyone in the Future of Medicine program

Manage patient-facing work for each assigned participant to deliver the highest quality customer experience within required program timelines

Understand and identify participants of the program who require more or less engagement, tailoring to their needs for a positive participant experience

Interpret patient lab results and medication use to determine pre-screening qualification for a study

Apply critical thinking to evaluate a participant's potential eligibility for a specific study

Communicate with participants of the program during routine check-ins after referring them to study sites

Analyze and understand study protocols to help match potential members with current and or upcoming study opportunities

Manage participant referral work across several clinical protocols simultaneously

Escalate potential issues that may arise and correctly follow program guides, SOPs, and other written instruction regarding escalations

Communicate via various mediums such as phone, email, and video conference

Document all patient interaction appropriately and in accordance with GCP and ALCOA-C

Adapt to study specific requirements and priorities, including alternative ways of handing off patient referrals to sites (direct schedule, warm transfer, etc.)

Follow-up and interact with study sites as needed to ensure referral pull-through

Consent

Perform the Informed Consent process with participants virtually by using e-consent technology

Review all elements of the consent form with the participant and assess their understanding to ensure the protection of human participants in clinical research. Complete signatures using the e-consent platform

General Patient Support

Manage participant communication via a call center software, texts, emails, and other platforms and systems

Assist participants who call into the central line and give them an optimal customer experience

Manage, update, and maintain participant activity in a dedicated tech management system in real time

Perform quality checks for self and others to ensure overall quality and integrity of data

Other Responsibilities

Work effectively and efficiently with other CSC-Rs, physicians, and sites

Collaborate, review, and provide feedback/input on the development of education materials for the program  

Identify and implement new ways of retaining and engaging potential study participants  

Complete ongoing trainings and adhere to system access guidelines. 

Speak about studies with patients in a manner they can understand

The Expertise Required

Able to flex as needed in a fast moving, fast paced environment while maintaining the companies' values and mission

Technologically proficient

Demonstrate professionalism in all situations and work effectively with a diverse group of individuals 

Understand when issues require escalation

Proficient in research terminology and basic medical terminology

Understand the overall clinical development paradigm and excellent working knowledge of government regulations, GCP, and ALCOA-C

Strong organization and time management skills

High attention to detail

Effective communication over phone (proper speaking volume, clarity, speech cadence)

Excellent customer service skills

Warm, personable approach in communicating with others both verbally and in writing

Ability to communicate the basics of clinical research related to patient education

Ability to work effectively in a remote environment within minimal supervision

Proper home office set-up including a private space for participant communication and high-speed internet (at minimum: 100MB up and 15 MB down, 5 GHz router) 

  Certifications/Licenses, Education, and Experience:      

Minimum Experience:

At least 2 years of relevant clinical research experience

Experience working on high volume screening studies

Experience with patient education and retention

Fluency in Spanish is a bonus

How We Work Together

Location : Remote within the United States. This role requires 100% of work to be performed in a remote office environment.

Travel : This is a remote position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.

Physical demands associated with this position Include : The ability to use keyboards and other computer equipment.

The expected pay range for this role is $65,000 - $75,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)

Paid Time Off (PTO) and Company Paid Holidays

100% Employer paid medical, dental, and vision insurance plan options

Health Savings Account and Flexible Spending Accounts

Bi-weekly HSA employer contribution

Company paid Short-Term Disability and Long-Term Disability

401(k) Retirement Plan, with Company Match 

 

Mandatory Employer Disclosures:

Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment. Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment. Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws. Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. 

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Diversity & Inclusion

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we 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 are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, 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 unable to sponsor work visas at this time.

If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com