Immediate opening for full time Patient Recruiter
Job Title: Participant Recruiter
Rainier Clinical Research Center (RCRC) was founded in 1991. Since that time, we have participated in more than 600 Phase I-IV clinical trials involving thousands of patients. The Patient Recruitment Coordinator contacts potential clinical trial participants, interviews them to see if they are eligible for research, and coordinates the recruitment for multiple projects (up to 40 a year). S/he ensures Rainier Clinical Research Center meets all of its required patient contract. This position is ideal for a sociable professional seeking a fast-paced, challenging career and is interested in health care.
Reports to: Recruitment Supervisor
Responsibilities:
RequirementsEducation & Experience
RequiredSkills:
Must be fully vaccinated for COVID-19
Must be willing to work at our office in Renton, WA
EEO Statement: Rainier Clinical Research Center is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Work Remotely
Benefits:
Company Education Allowance:
Schedule:
Compensation:$18 - $25 per hour
Supplemental Pay:
Bonus pay
Work Location: One location
Job Type: Full-time
Supplemental pay types:
Ability to commute/relocate:
Education:
Language:
Shift availability:
Work Location: One location
Immediate opening for a full time General Administrative Assistant
Job description
Rainier Clinical Research Center (Renton, WA) is seeking a full time General Administrative Assistant. The General Administrative Assistant position includes front desk duties and other duties that support the administrative department.
Rainier Clinical Research Center is a privately-owned clinical research center conducting clinical trials for pharmaceutical, biotech and device companies. The company has been in business for over 30 years with a specialty in diabetes research. All studies are conducted under the supervision of board-certified physicians.
We are currently seeking a full-time General Administrative Assistant with excellent attention to detail and the ability to work in a fast-paced work atmosphere.
Primary Responsibilities:
Required Skills/Abilities:
Education and Experience:
Physical Requirements:
Must be fully vaccinated for COVID-19
Job Type: Full-time
Salary: $18 - $23.50 per hour
Supplemental pay:
Benefits:
Company Education Allowance:
Work Remotely: No
Schedule:
Work Location: One location
Immediate full time job opening for a large multi-specialty research center specializing in metabolic disorders. We conduct research studies of investigational medications and devices for pharmaceutical and biotech companies with an emphasis in diabetes, lipids and obesity. The Clinical Research Coordinator, under the supervision of the Principal Investigator, executes and coordinates daily clinical research activities and performs necessary functions for the conduct of clinical studies according to ICH/GCP guidelines and FDA regulations
Clinical Research Coordinator (Experienced)
Rainier Clinical Research Center – Renton, WA 98057
CLINICALRESEARCH COORDINATOR (Experienced): Immediate full time job opening for a large multi-specialty research center specializing in metabolic disorders. We conduct research studies of investigational medications and devices for pharmaceutical and biotech companies with an emphasis in diabetes, lipids and obesity.
The Clinical Research Coordinator, under the supervision of the Principal Investigator, executes and coordinates daily clinical research activities and performs necessary functions for the conduct of clinical studies according to ICH/GCP guidelines and FDA regulations
Responsibilities:
Requirements:
1. Study Start-up
·Attend Investigator Meetings
·Work with recruitment team to develop a recruiting strategy
·Develop source documents according to SOPs
·Obtain proper training on study specific procedures and documents
·Ensure staff completion of proper training on study specific procedures and documents
Become thoroughly knowledgeable with assigned protocols
a. Inclusion/Exclusion criteria
b. Allowed/disallowed medications
c. Procedure requirements (Labs, ECGs, etc)
d. Patient visit requirements
e. Proper medication dispensing and titrations
2. Manage All Aspects of Conducting Clinical Trial
·Properly consent the patients
·Certify that all study related procedures are done according to protocol
·Ensure that Case Report Forms (CRFs) and other documentation are done according to protocol
·Confirm that Investigational product is dispensed and returned properly
·Verify patient compliance to protocol
·Work with Clinical Research Associate (CRA)/Monitor to resolve queries and corrections
·Function as a liaison between patient, RCRC, Investigator, and sponsor
·Follow Good Clinical Practices Guidelines
·Work closely with Investigators to ensure patient safety and compliance
·Coordinator understands and comply FDA regulations and able apply those effectively
·Coordinator shows a basic sense of responsibility for their studies.
·Disclaimer: May be asked to do other not listed tasks as well.
·Able to manage higher level studies requiring more advance interaction with patient and physician for example insulin titration.
·Able to develop and lead a team to optimize coordination with their studies.
4.Study Completion
·Ensure that all data is submitted to the sponsor
·Work with CRA/Monitor to resolve outstanding issues
Job Type: Full-time
Required experience: Clinical Research Coordinator work experience required.
Benefits:
Company Education Allowance:
Job Type: Full-time
Medical specialties:
Schedule:
Supplemental pay types:
Ability to commute/relocate:
Education:
Shift availability:
Work Location: One location
Job Type: Full-time
Ability to commute/relocate:
Work Location: One location
Immediate part time opening for a Registered Dietitian
REGISTERED DIETITIAN
Rainier Clinical Research Center (Renton, WA) has a part-time job opening for a Registered Dietician for a large multi-specialty research center specializing in metabolic disorders. We conduct research studies of investigational medications and devices for pharmaceutical and biotech companies with an emphasis in diabetes, lipids, and obesity.
The Registered Dietician will provide hands on patient nutrition counseling for participants in a clinical research study(s). The role may include handling of study information, applications and medical devices.
· What does the nutrition content look like?
Responsibilities:
Performing study related procedures including but not limited to:
-Administering Informed Consent Forms to study participants
-Taking EKG's and vital signs
-Completing all study-related documents in a timely manner
-Ensure Patient Compliance to Study Protocol
-Ensure that GCP and FDA guidelines are followed
-Schedule and coordinate all dietary consult related visits and procedures with other departments as required by study protocol
-Work with sponsoring pharmaceutical or biotech company to ensure that all dietary consults required duties are completed according to sponsor guidelines
-Keep principal investigator informed of study participant progress and changes to protocol or dietary consult study procedures
-Dispense and account for investigational drug administered during the study
- Provide nutritional counseling to study participants
Requirements:
-Must have excellent communication skills
-Must be highly organized with great attention to detail
-Must thrive in a fast-paced environment and be able to multi-task
-Must be highly self-motivated
-Bachelor's Degree in Nutrition/Dietetics and have a current RD certification
-Experience with diabetes or diabetes education preferred
Benefits:
Company EducationAllowance:
Job Type: Part-time
Salary: $49,885.00 -$72,687.00 per year
Supplemental pay types:
Medical specialties:
Schedule:
Ability to commute/relocate:
Education:
License/Certification:
Shift availability:
Work Location: Onelocation
- Jeff Klaff, Human Resources Specialist