CLINICAL TRIALS Registered Dietitian- PART TIME (5-20+ hrs/week)
We are seeking a dedicated and professional Registered Dietitian who can understand and follow institutional Standard Operating Procedures (SOPs), review and assess protocols for clarity and feasibility, and ensure all training and study requirements are met prior to trial conduct.
The candidate will work under the supervision of the Principal Investigator(s) while exercising excellent clinical judgment in patient monitoring and care.
This role requires timely communication with internal teams, investigators, review boards, and study subjects.
The position involves performing protocol-mandated visits, providing personalized Lifestyle Management Counseling, and delivering educational materials to assist patients in achieving their nutritional and physical activity goals.
Additionally, the candidate will attend remote protocol visits, perform patient diet and nutritional education, schedule study visits, prepare documentation, and participate in quality improvement projects.
Part time role: 5-20+ hours per week
Responsibilities
Understand and follow institutional SOPs.
Review and assess protocol for clarity and logistical feasibility.
Ensure all training and study requirements are met prior to trial conduct.
Work under the supervision of Principal Investigator(s) while exercising excellent clinical judgment.
Communicate timely with internal teams, investigators, review boards, and study subjects.
Perform protocol-mandated visits, including providing personalized Lifestyle Management Counseling.
Provide helpful materials to assist patients in achieving their nutritional and physical activity goals.
Attend remote, video-assisted protocol visits.
Review applicable study logs, collect AE/Concomitant Medication changes, and complete eSource.
Perform patient diet and nutritional education.
Schedule study visits with participants within the protocol window.
Prepare documentation ahead of appointments and ensure study participant files and source documents are ready.
Participate and implement quality improvement projects.
Additional duties and responsibilities as assigned.
Pay and Benefits
The pay range for this position is $25.00 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully remote position.
Application Deadline
This position is anticipated to close on Jun 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.