Travel Sub-Investigator

Job Description

Job Description

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 

How This Role Makes a Difference

The Sub-Investigator will be responsible for travel mixed with remote tele-medicine work to support our clinical research studies.  Additionally, our Sub-Investigator will be skilled in administering investigational products (IV, SC, TD, IM, PO administration), performing physical examinations, monitoring for investigational product related reactions, among other duties beyond the standard clinical research Sub-Investigator role. Care Access is looking for highly motivated Nurse Practitioners or Physician's Assistants to support clinical trial related activities in states throughout the USA.  

How You'll Make An Impact

• Clinical Research Patient Care & Study Procedures
  • Conduct study visits; perform physical exams; administer investigational products (oral, IV, IM, SQ, transdermal); perform phlebotomy, IV placement, vital signs, ECGs, specimen collection/processing ; monitor participants throughout the study; educate participants on study medications; provide direct clinical care and maintain a safe clinical environment. 
• Protocol Compliance & Regulatory Oversight
  • Ensure compliance with study protocols, GCP, SOPs, IRB requirements, OSHA standards, and applicable regulations; review informed consent, protocol, and investigator brochure; complete and sign study documentation; oversee delegated study activities and ensure accurate documentation. 
• Medical Oversight & Safety Monitoring
  • Assess and manage adverse events and infusion reactions; review laboratory and clinical data for medical significance; provide medical management of study participants; evaluate eligibility, approve enrollment/randomization, and ensure timely reporting of serious adverse events to the Principal Investigator. 
• Study Coordination & Communication 
• Collaborate with the Principal Investigator and research team; communicate with study participants, sponsors, IRBs, and internal departments; attend meetings; support subject recruitment, prescreening, scheduling, and coordination of study activities. 
• Training, Leadership & Administrative Responsibilities
  • Train and mentor clinical staff on study procedures; delegate responsibilities appropriately; maintain clinical readiness; participate in quality improvement activities; complete required documentation and perform other assigned duties. 

The Expertise Required

• Ability to check, perform, and document vitals as well as EKG (ECG)   
• Phlebotomy and expert IV skills  
• 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 with good understanding of medical terminology.  
• Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors.  
• 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, innovative, and able to take thoughtful risks while communicating concerns and mitigations.    
• Good management and organizational skills, understanding of medical procedures.   
• Exceptional interpersonal skills, willingness to the ability to work independently.   
• Ability to lift a minimum of 50 pounds.   
• Command of professional and Business English (written and spoken).   
• You must have the authorization to work in the US for any employer.   
• You must not need visa sponsorship, either now or in the future.  
• You must live in the USA and be willing and able to travel with 24–36-hour notice  

Certifications/Licenses, Education, and Experience:

• Minimum Education:
  • At least Master's Level Science Degree.  Nurse Practitioner or Physician Assistant with 5+ years of clinical experience.  
  • Must hold active, unrestricted licensure in at least 10 U.S. states and be willing and able to obtain additional state licenses as needed. 
• Minimum Experience:
  • Clinical practice experience desired with infusion skillset.  
  • A minimum of 1 year of relevant work experience as Sub-Investigator (preferred) in a Clinical Research setting.  
  • Preferred at least one (1) year of experience as a Clinical Research Coordinator or willingness to learn.  

 

How We Work Together

• Location : This is an on-site mixed with remote tele-medicine work position.
• Travel : Regional and nationwide travel requirements up to 100% dependent on project design and business need. Regularly planned travel will be required as part of the role. 
• Physical demands associated with this position Include : The ability to use keyboards and other computer equipment.
  • Walking 10%, Standing 30%, Sitting 50%, Lifting up to and overhead 25 lbs.

The expected pay range for this role is $130,000 - $165,000 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: View email address on us.fitly.work