Clinical Research Coordinator - II
20–22 an hour
Behavioral Health Market Context
Apply Nowvia Indeed
Benefits
Dental CoveragePaid Time OffHealth Insurance
Job Description
borative work environment with room for professional growth.
Job description
The Clinical Research Coordinator's primary responsibility is to provide assistance with clinical research studies being conducted on site. The Clinical Research Coordinator II helps manage elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines, and company standard operating procedures. These elements include but are not limited to assisting with the day-to-day management of a study and study closure activities.
Responsibilities:
• Helps in the recruitment of study subjects
• Aides in assessing eligibility of patients for participation in protocols
• Participates in the administration of informed consent process
• Assists with the collection, entering, maintenance of data
• Reviews data and progress notes with CRCs and principal investigator
• Prepares study files for data
• Prepares lab kits for upcoming research visits
• Processes blood and urine samples for shipping
• Perform back-up study coordination if needed by trial schedule
The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this position. It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision.
Other information:
-1 year experience in clinical research or health care field preferred
-Understanding of medical terminology and clinical trials preferred
-Phlebotomy experience strongly preferred
-CMA preferred
Skills required:
• Working knowledge of PCs and word processing and data management software
• Verbal and written communication
• Goal-oriented; self-directive
• Initiation, motivation, creativity
• Organizational and interpersonal
• Ability to actively participate as a team player
Experience:
• Phlebotomy: 1 year (Preferred)
• Clinical research: 1 year (Required)
Work Location: In person
Join our team as a Clinical Research Coordinator and contribute to our mission of delivering exceptional healthcare services. If you are passionate about making a difference in the healthcare industry and possess the required skills, we invite you to apply today to be part of our dedicated team. Please email cover letter and resume to [email protected]
Job Type: Full-time
Pay: $20.00 - $22.00 per hour
Benefits:
• 401(k)
• Dental insurance
• Employee assistance program
• Employee discount
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance
Medical Specialty:
• Gastroenterology
Work Location: In person
Job description
The Clinical Research Coordinator's primary responsibility is to provide assistance with clinical research studies being conducted on site. The Clinical Research Coordinator II helps manage elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines, and company standard operating procedures. These elements include but are not limited to assisting with the day-to-day management of a study and study closure activities.
Responsibilities:
• Helps in the recruitment of study subjects
• Aides in assessing eligibility of patients for participation in protocols
• Participates in the administration of informed consent process
• Assists with the collection, entering, maintenance of data
• Reviews data and progress notes with CRCs and principal investigator
• Prepares study files for data
• Prepares lab kits for upcoming research visits
• Processes blood and urine samples for shipping
• Perform back-up study coordination if needed by trial schedule
The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this position. It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision.
Other information:
-1 year experience in clinical research or health care field preferred
-Understanding of medical terminology and clinical trials preferred
-Phlebotomy experience strongly preferred
-CMA preferred
Skills required:
• Working knowledge of PCs and word processing and data management software
• Verbal and written communication
• Goal-oriented; self-directive
• Initiation, motivation, creativity
• Organizational and interpersonal
• Ability to actively participate as a team player
Experience:
• Phlebotomy: 1 year (Preferred)
• Clinical research: 1 year (Required)
Work Location: In person
Join our team as a Clinical Research Coordinator and contribute to our mission of delivering exceptional healthcare services. If you are passionate about making a difference in the healthcare industry and possess the required skills, we invite you to apply today to be part of our dedicated team. Please email cover letter and resume to [email protected]
Job Type: Full-time
Pay: $20.00 - $22.00 per hour
Benefits:
• 401(k)
• Dental insurance
• Employee assistance program
• Employee discount
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance
Medical Specialty:
• Gastroenterology
Work Location: In person
Qualifications
- •Working knowledge of PCs and word processing and data management software
- •Verbal and written communication
- •Goal-oriented; self-directive
- •Initiation, motivation, creativity
- •Organizational and interpersonal
- •Ability to actively participate as a team player
- •Clinical research: 1 year (Required)
- •Gastroenterology
Benefits
- •Pay: $20.00 - $22.00 per hour
- •401(k)
- •Dental insurance
- •Employee assistance program
- •Employee discount
- •Health insurance
- •Health savings account
- •Life insurance
- •Paid time off
- •Vision insurance
Responsibilities
- •The Clinical Research Coordinator's primary responsibility is to provide assistance with clinical research studies being conducted on site
- •The Clinical Research Coordinator II helps manage elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines, and company standard operating procedures
- •These elements include but are not limited to assisting with the day-to-day management of a study and study closure activities
- •Helps in the recruitment of study subjects
- •Aides in assessing eligibility of patients for participation in protocols
- •Participates in the administration of informed consent process
- •Assists with the collection, entering, maintenance of data
- •Reviews data and progress notes with CRCs and principal investigator
- •Prepares study files for data
- •Prepares lab kits for upcoming research visits
- •Processes blood and urine samples for shipping
- •Perform back-up study coordination if needed by trial schedule
- •The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this position
More Jobs
- Operations Manager, ABA Therapy Centerat Confidential
- Speech Pathologistat Encompass Health Rehabilitation Hospital of North Memphis
- ABA Therapist - Flexible Hours | Clayat BK Behavior Ventures
- Speech-Language Pathologist - Flexible Pay & Benefitsat Tate Springs Health & Rehab
- Registered Behavior Technician — ABA Therapyat Flourish Specialty Services
- Behavior Change Specialist - Dayton, OHat BK Behavior
- Registered Behavior Technician; RBTat Skill Builders ABA
- Enrollment Delivery Lead AI-Powered Clinical Trialsat Massive Bio
- ABA Supervisor Plano, Texas, United Statesat Cortica Inc
- Behavior Technician- Entry Levelat Training Wheels ABA