Research Assistant/Coordinator
South Euclid, OHFull-time
Behavioral Health Market Context
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Benefits
Paid Time OffDental CoverageHealth Insurance
Job Description
costeroids. The Research Assistant/Coordinator will enjoy being a member of a dynamic and enthusiastic team of research professionals who oversee research services here at Senders Pediatrics.
Some responsibilities of the Research Assistant/Coordinator include:
• To ensure the safe and ethical conduct of clinical research as well as compliance with the International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) regulatory requirements.
• To recruit subjects for clinical studies by making phone calls, sending mailings and discussing studies with parents and potential participants.
• To become proficient in study start up, ongoing study management including data capture and adverse event processing and study close out requirements.
• To become proficient in phlebotomy the accurate processing of blood, sera and other biological specimens and the administration of vaccines.
• To develop excellent time management, organization, planning and prioritization skills critical to the successful management of multiple clinical trials.
• To interact with research sponsors and their representatives in a positive, ethical and productive manner.
• To interface with the clinical staff, including front office, medical assistants and providers in promoting the activities of the research department.
• To be willing to participate in other research-related duties that may be assigned
Knowledge, skills and experience required:
• Bachelor’s Degree in the sciences or related area is required
• Minimum 1 year in Clinical Research, or recent college grad with biology major and strong interest in clinical research
• Phlebotomy skills and confidence in vaccine administration are preferred although we are willing to train
• Competence with computers, databases and the MS office suite
• Possesses a growth mindset
• Takes a team approach to work
• Willingness to be challenged and to gain mastery in new areas
• Maintains close attention to detail in all work related areas
Job Type: Full-time
Pay: From $20.00 per hour
Benefits:
• Dental insurance
• Employee assistance program
• Employee discount
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance
Education:
• Bachelor's (Preferred)
Work Location: In person
Some responsibilities of the Research Assistant/Coordinator include:
• To ensure the safe and ethical conduct of clinical research as well as compliance with the International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) regulatory requirements.
• To recruit subjects for clinical studies by making phone calls, sending mailings and discussing studies with parents and potential participants.
• To become proficient in study start up, ongoing study management including data capture and adverse event processing and study close out requirements.
• To become proficient in phlebotomy the accurate processing of blood, sera and other biological specimens and the administration of vaccines.
• To develop excellent time management, organization, planning and prioritization skills critical to the successful management of multiple clinical trials.
• To interact with research sponsors and their representatives in a positive, ethical and productive manner.
• To interface with the clinical staff, including front office, medical assistants and providers in promoting the activities of the research department.
• To be willing to participate in other research-related duties that may be assigned
Knowledge, skills and experience required:
• Bachelor’s Degree in the sciences or related area is required
• Minimum 1 year in Clinical Research, or recent college grad with biology major and strong interest in clinical research
• Phlebotomy skills and confidence in vaccine administration are preferred although we are willing to train
• Competence with computers, databases and the MS office suite
• Possesses a growth mindset
• Takes a team approach to work
• Willingness to be challenged and to gain mastery in new areas
• Maintains close attention to detail in all work related areas
Job Type: Full-time
Pay: From $20.00 per hour
Benefits:
• Dental insurance
• Employee assistance program
• Employee discount
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance
Education:
• Bachelor's (Preferred)
Work Location: In person
Qualifications
- •Bachelor’s Degree in the sciences or related area is required
- •Minimum 1 year in Clinical Research, or recent college grad with biology major and strong interest in clinical research
- •Competence with computers, databases and the MS office suite
- •Possesses a growth mindset
- •Takes a team approach to work
- •Willingness to be challenged and to gain mastery in new areas
- •Maintains close attention to detail in all work related areas
Benefits
- •Pay: From $20.00 per hour
- •Dental insurance
- •Employee assistance program
- •Employee discount
- •Health insurance
- •Health savings account
- •Life insurance
- •Paid time off
- •Retirement plan
- •Vision insurance
Responsibilities
- •The Research Assistant/Coordinator will enjoy being a member of a dynamic and enthusiastic team of research professionals who oversee research services here at Senders Pediatrics
- •To ensure the safe and ethical conduct of clinical research as well as compliance with the International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) regulatory requirements
- •To recruit subjects for clinical studies by making phone calls, sending mailings and discussing studies with parents and potential participants
- •To become proficient in study start up, ongoing study management including data capture and adverse event processing and study close out requirements
- •To become proficient in phlebotomy the accurate processing of blood, sera and other biological specimens and the administration of vaccines
- •To develop excellent time management, organization, planning and prioritization skills critical to the successful management of multiple clinical trials
- •To interact with research sponsors and their representatives in a positive, ethical and productive manner
- •To interface with the clinical staff, including front office, medical assistants and providers in promoting the activities of the research department
- •To be willing to participate in other research-related duties that may be assigned
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