<p>Location: Memphis, TN</p><br/><p>Employment Type: Full Time - Regular</p><br/><p>Team: Site Conduct</p><br/><div><b style="font-size: 15pt;">Sub-Investigator</b></div><div><span style="font-size: 12pt;">Department: US Site Network</span></div><div><span style="font-size: 12pt;">Level:&nbsp; Individual Contributor</span></div><div><span style="font-size: 12pt;">Work Location: On Site</span></div><div><span style="font-size: 12pt;">Updated Last: 09/27/2024</span></div><div>______________________________________________________________________________________</div><div><b style="font-size: 13pt;">&nbsp;</b></div><div><b style="font-size: 13pt;">What We Do</b></div><div><span style="font-size: 12pt;">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.</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 Sub-Investigator will be responsible for regional travel mixed with remote tele-medicine work to support our clinical research. Care Access is looking for Nurse Practitioners or Physicians Assistants to support clinical trial related activities in states throughout the USA.</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><b style="font-size: 13pt;">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; </span><span style="font-size: 12pt;">Work closely with the Principal Investigator to oversee the execution of study protocols, delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols, study-specific laboratory procedures, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures, OSHA guidelines, and other state and local regulations as applicable </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Attends and participates in meetings with the director, other managers, and staff as necessary </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Complies with regulatory requirements, policies, procedures, and standards of practice </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Read and understand the informed consent form, protocol, and investigator's brochure </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Be available to see subjects virtually or in-person as dictated by project design, answer their questions, and resolve medical issues during the study visit </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Sign and ensure that the study documentation for each study visit is completed </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Perform all study responsibilities in compliance with the IRB approved protocol </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Review screening documentation and approves subjects for admission to study </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Review admission documentation and approves subject for randomization </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Provide ongoing assessment of the study subject/patient to identify Adverse Events </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Ensure that serious and unexpected adverse events are reported promptly to the Pl </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Review and evaluates all study data and comments to the clinical significance of any out of range results </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Perform physical examinations as part of screening evaluation and active study </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Conduct </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Provide medical management of adverse events as appropriate </span></div><div><span style="font-size: 12pt;">*Perform other duties as trained for and assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.</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 on-site 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;">Knowledge, Skills and Abilities:</span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&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; </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; </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; </span><span style="font-size: 12pt;">Strong organizational skills: Able to prioritize, support, and follow through on assignments </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Team Collaboration Skills: Work effectively and collaboratively with other team members to accomplish mutual goals. Bring positive and supportive attitude to achieving these goals </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&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; </span><span style="font-size: 12pt;">Ability to balance tasks with competing priorities </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&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; </span><span style="font-size: 12pt;">Curiosity and passion to learn, innovate, able to take thoughtful risks and get things done </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&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; </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; </span><span style="font-size: 12pt;">Ability to work independently in a fast-paced environment with minimal supervision </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Must have a client service mentality </span></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><span style="font-size: 12pt;">Certifications/Licenses, Education, and Experience:</span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Nurse Practitioner or Physician Assistant with 5+ years of clinical experience </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Currently licensed in good standing in one or more states listed above </span></div><div><span style="font-size: 12pt;">●</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">A minimum of 1 year of relevant work experience as Sub-Investigator (preferred) in a Clinical Research setting</span></div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><b style="font-size: 13pt;">Benefits (US Full-Time Employees Only)</b></div><div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Paid Time Off (PTO) and Company Paid Holidays</div><div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>100% Employer paid medical, dental, and vision insurance plan options</div><div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Health Savings Account and Flexible Spending Accounts</div><div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Bi-weekly HSA employer contribution</div><div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Company paid Short-Term Disability and Long-Term Disability</div><div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>401(k) Retirement Plan, with Company Match&nbsp;</div><div><span style="font-size: 12pt;">&nbsp;</span></div><div><b style="font-size: 13pt;">Diversity &amp; Inclusion</b></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. </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 best</span></div><div><span style="font-size: 12pt;">physicians and caring for patients. Our team of experts is paving the way to take this vision forward through innovation and a unique technology-enabled.</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.</span></div><div>&nbsp;</div><div><span style="font-size: 10.5pt;">&nbsp;</span><span style="font-size: 16px;">Care Access is unable to sponsor work visas at this time.</span></div><div><span style="font-size: 12pt;">&nbsp;</span></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>&nbsp;</div><div>&nbsp;</div><div>&nbsp;</div><div>&nbsp;</div><div>&nbsp;</div><div>&nbsp;</div>

Location: Memphis, TN

  

Employment Type: Full Time - Regular

  

Team: Site Conduct

  

 **Sub-Investigator**

Department: US Site Network

Level:  Individual Contributor

Work Location: On Site

Updated Last: 09/27/2024

______________________________________________________________________________________

 ** **

 **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 Sub-Investigator will be responsible for regional travel mixed with remote
tele-medicine work to support our clinical research. Care Access is looking
for Nurse Practitioners or Physicians Assistants to support clinical trial
related activities in states throughout the USA.



 **What You'll Be Working On**

 **Duties include but not limited to:**

●      Work closely with the Principal Investigator to oversee the execution
of study protocols, delegating study related duties to site staff, as
appropriate, and ensuring site compliance with study protocols, study-specific
laboratory procedures, standards of Good Clinical Practice (GCP), Standard
Operating Procedures (SOPs), quality (QA/QC) procedures, OSHA guidelines, and
other state and local regulations as applicable

●      Attends and participates in meetings with the director, other managers,
and staff as necessary

●      Complies with regulatory requirements, policies, procedures, and
standards of practice

●      Read and understand the informed consent form, protocol, and
investigator's brochure

●      Be available to see subjects virtually or in-person as dictated by
project design, answer their questions, and resolve medical issues during the
study visit

●      Sign and ensure that the study documentation for each study visit is
completed

●      Perform all study responsibilities in compliance with the IRB approved
protocol

●      Review screening documentation and approves subjects for admission to
study

●      Review admission documentation and approves subject for randomization

●      Provide ongoing assessment of the study subject/patient to identify
Adverse Events

●      Ensure that serious and unexpected adverse events are reported promptly
to the Pl

●      Review and evaluates all study data and comments to the clinical
significance of any out of range results

●      Perform physical examinations as part of screening evaluation and
active study

●      Conduct

●      Provide medical management of adverse events as appropriate

*Perform other duties as trained for and 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.



 **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 skills: Able to prioritize, support, and follow
through on assignments

●      Communication Skills: Strong verbal and written communication skills as
evidenced by positive interactions with coworkers, management, clients and
vendors

●      Team Collaboration Skills: Work effectively and collaboratively with
other team members to accomplish mutual goals. Bring positive and supportive
attitude to achieving these goals

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

●      Ability to balance tasks with competing priorities

●      Critical thinker and problem solver

●      Curiosity and passion to learn, innovate, able to take thoughtful risks
and get things done

●      Friendly, outgoing personality; maintain a positive attitude under
pressure

●      High level of self-motivation and energy

●      Ability to work independently in a fast-paced environment with minimal
supervision

●      Must have a client service mentality



Certifications/Licenses, Education, and Experience:

●      Nurse Practitioner or Physician Assistant with 5+ years of clinical
experience

●      Currently licensed in good standing in one or more states listed above

●      A minimum of 1 year of relevant work experience as Sub-Investigator
(preferred) in a Clinical Research setting



 **Benefits (US Full-Time Employees Only)**

·        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



 **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 best

physicians and caring for patients. Our team of experts is paving the way to
take this vision forward through innovation and a unique technology-enabled.



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 unable to sponsor work visas at this time.



 **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.













