<p>Location: New Orleans, LA</p><br/><p>Employment Type: Part Time -  Temporary</p><br/><p>Team: Site Support Solutions</p><br/><div><b style="font-size: 13pt;">What We Do</b></div><div><span style="font-size: 12pt;">Care Access is a unique, multi-specialty network of research sites which operates as one connected team of physician investigators, nurse coordinators, and operations managers. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.</span></div><div><span style="font-size: 10.5pt;">&nbsp;</span></div><div><b style="font-size: 13pt;">Who We Are</b></div><div><span style="font-size: 12pt;">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. </span></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><b style="font-size: 13pt;">Position Overview</b></div><div><span style="font-size: 12pt;">The Clinical Research Coordinator (CRC) position delivers strong customer experience for both sites and patients by providing onsite or remote study support under the delegation of a PI. The CRC is responsible for study coordination, including study start-up, patient recruitment, backup support, and other duties as required to support the clinical trial and site. This position is an onsite, hourly, part time role at approximately 24 hours a week. </span></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><b style="font-size: 13pt;">What You'll Be Working On</b></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><b style="font-size: 12pt;">Duties include but not limited to:</b></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;</span><span style="font-size: 12pt;">Ability to understand and follow institutional SOPs</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Review and assess protocol (including amendments) for clarity, logistical feasibility</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Ensure that all training and study requirements are met prior to trial conduct</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Work under the supervision of the Principal Investigator(s), while exercising excellent clinical judgment in patient monitoring and care</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Timely communications with internal teams, investigators, review boards, and study subjects</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Obtain Informed Consent Form per SOPs</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Perform protocol mandated visits which may include collecting study participant health assessments (e.g. vitals, ECG) and biospecimens (e.g. labs)&nbsp;</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Provide study medication per protocol to study participants&nbsp;</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Complete case report forms and query resolution&nbsp;</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Recruit study patients by calling subjects from database and potential volunteers (phone, email, post, etc.) and document contact accordingly &nbsp;</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Request medical records of potential and current study participants </span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Perform patient education  &nbsp;</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Schedule study visits with study participants, contact with reminders  &nbsp;</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Prepare documentation ahead of appointment; Ensure study participant files and source documents are ready for their visit &nbsp;</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Additional duties/responsibilities may be assigned as needed</span></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><b style="font-size: 13pt;">Physical and Travel Requirements</b></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">This is an onsite position with regional commute requirements. Regularly planned travel within the region will be required as part of the role.</span></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><b style="font-size: 13pt;">What You Bring</b></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><b style="font-size: 12pt;">Knowledge, Skills, and Abilities:</b></div><div><span style="font-size: 7pt;">&nbsp;</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Excellent working knowledge of medical and research terminology</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Excellent working knowledge of federal regulations, good clinical practices (GCP)</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Ability to communicate and work effectively with a diverse team of professionals.</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Critical thinker and problem solver</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Friendly, outgoing personality; maintain a positive attitude under pressure.</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">High level of self-motivation and energy</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Excellent professional writing and communication skills</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Ability to work independently in a fast-paced environment with minimal supervision.</span><b style="font-size: 12pt;">&nbsp;</b></div><div><b style="font-size: 12pt;">&nbsp;</b></div><div><b style="font-size: 12pt;">Certifications/Licenses, Education, and Experience:</b></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Bachelor’s Degree preferred, or equivalent combination of education, training and experience.</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">A minimum of 2-3 years prior Clinical Research Coordinator experience required</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Requires: ability to work onsite in New Orleans, LA</span></div><div><span style="font-size: 12pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Experience with Hepatology preferred</span></div><div><b style="font-size: 13pt;">Diversity &amp; Inclusion</b><span style="font-size: 13pt;">&nbsp;</span></div><div><span style="font-size: 12pt;">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.&nbsp;&nbsp;</span></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><span style="font-size: 12pt;">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&nbsp;</span></div><div><span style="font-size: 12pt;">physicians and caring for patients.&nbsp;</span></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><span style="font-size: 12pt;">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.&nbsp;</span></div><div><span style="font-size: 11pt;">&nbsp;</span></div><div><b style="font-size: 12pt;">Care Access is currently unable to sponsor work visas.&nbsp;</b></div><div><br></div><div><b style="font-size: 13pt;">Employment Statement</b></div><div><span style="font-size: 11.5pt;">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.</span></div><div><br></div>

Location: New Orleans, LA

  

Employment Type: Part Time - Temporary

  

Team: Site Support Solutions

  

 **What We Do**

Care Access is a unique, multi-specialty network of research sites which
operates as one connected team of physician investigators, nurse coordinators,
and operations managers. 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 Coordinator (CRC) position delivers strong customer
experience for both sites and patients by providing onsite or remote study
support under the delegation of a PI. The CRC is responsible for study
coordination, including study start-up, patient recruitment, backup support,
and other duties as required to support the clinical trial and site. This
position is an onsite, hourly, part time role at approximately 24 hours a
week.



 **What You'll Be Working On**



 **Duties include but not limited to:**

·        Ability to understand and follow institutional SOPs

·       Review and assess protocol (including amendments) for clarity,
logistical feasibility

·       Ensure that all training and study requirements are met prior to trial
conduct

·       Work under the supervision of the Principal Investigator(s), while
exercising excellent clinical judgment in patient monitoring and care

·       Timely communications with internal teams, investigators, review
boards, and study subjects

·       Obtain Informed Consent Form per SOPs

·       Perform protocol mandated visits which may include collecting study
participant health assessments (e.g. vitals, ECG) and biospecimens (e.g. labs)

·       Provide study medication per protocol to study participants

·       Complete case report forms and query resolution

·       Recruit study patients by calling subjects from database and potential
volunteers (phone, email, post, etc.) and document contact accordingly  

·       Request medical records of potential and current study participants

·       Perform patient education  

·       Schedule study visits with study participants, contact with reminders  

·       Prepare documentation ahead of appointment; Ensure study participant
files and source documents are ready for their visit  

·       Additional duties/responsibilities may be assigned as needed



 **Physical and Travel Requirements**

·       This is an onsite position with regional commute requirements.
Regularly planned travel within the region will be required as part of the
role.



 **What You Bring**



 **Knowledge, Skills, and Abilities:**



·       Excellent working knowledge of medical and research terminology

·       Excellent working knowledge of federal regulations, good clinical
practices (GCP)

·       Ability to communicate and work effectively with a diverse team of
professionals.

·       Strong organizational, prioritization and leadership skills and
capabilities with a strong attention to detail

·       Strong computer skills with demonstrated abilities using clinical
trials database, IVR systems, electronic data capture, MS word and excel.

·       Critical thinker and problem solver

·       Friendly, outgoing personality; maintain a positive attitude under
pressure.

·       High level of self-motivation and energy

·       Excellent professional writing and communication skills

·       Ability to work independently in a fast-paced environment with minimal
supervision. ** **

 ** **

 **Certifications/Licenses, Education, and Experience:**

·       Bachelor’s Degree preferred, or equivalent combination of education,
training and experience.

·       A minimum of 2-3 years prior Clinical Research Coordinator experience
required

·       Requires: ability to work onsite in New Orleans, LA

·       Experience with Hepatology preferred

 **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.

  

