Clinical Research Coordinator
Respiratory Medicine Research Institute of Michigan, PLC
Behavioral Health Market Context
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Benefits
Paid Time OffHealth InsuranceDental Coverage
Job Description
pecimen collection and processing), data review and entry, medication administration and accountability, patient education, administration of questionnaires, and completion of source documentation
• Learning of numerous clinical trial protocols
• Communication with patients, sponsors, and all other vendors associated with a clinical trial
• Resolving data entry queries
• Participating in monitoring visits
• Occasional travel out of state for investigator meetings
• Preparing for and participating in sponsor and federal audits
• Completing, reviewing, and maintaining regulatory documents
Education/Experience:
• Degree in a health-related field (RN, LPN, medical assistant, etc.)
• Strongly prefer - experience in clinical research, but are willing to train
• Excellent patient bedside manner
• Experience in phlebotomy
• Computer skills (MS Office, data entry)
• General knowledge of prescription medications
• Knowledge of medical terminology
• Excellent communication skills, verbal, and written
• Ability to work in a team setting and individually
• Ability to work in a setting with multiple deadlines and requirement to multitask
Job Type: Full-time
Benefits:
• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance
Ability to Commute:
• Ypsilanti, MI (Required)
Work Location: In person
• Learning of numerous clinical trial protocols
• Communication with patients, sponsors, and all other vendors associated with a clinical trial
• Resolving data entry queries
• Participating in monitoring visits
• Occasional travel out of state for investigator meetings
• Preparing for and participating in sponsor and federal audits
• Completing, reviewing, and maintaining regulatory documents
Education/Experience:
• Degree in a health-related field (RN, LPN, medical assistant, etc.)
• Strongly prefer - experience in clinical research, but are willing to train
• Excellent patient bedside manner
• Experience in phlebotomy
• Computer skills (MS Office, data entry)
• General knowledge of prescription medications
• Knowledge of medical terminology
• Excellent communication skills, verbal, and written
• Ability to work in a team setting and individually
• Ability to work in a setting with multiple deadlines and requirement to multitask
Job Type: Full-time
Benefits:
• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance
Ability to Commute:
• Ypsilanti, MI (Required)
Work Location: In person
Qualifications
- •Degree in a health-related field (RN, LPN, medical assistant, etc.)
- •Strongly prefer - experience in clinical research, but are willing to train
- •Excellent patient bedside manner
- •Experience in phlebotomy
- •Computer skills (MS Office, data entry)
- •General knowledge of prescription medications
- •Knowledge of medical terminology
- •Excellent communication skills, verbal, and written
- •Ability to work in a team setting and individually
- •Ability to work in a setting with multiple deadlines and requirement to multitask
- •Ability to Commute:
- •Ypsilanti, MI (Required)
Benefits
- •401(k)
- •Dental insurance
- •Health insurance
- •Paid time off
- •Vision insurance
Responsibilities
- •Allergy and asthma research site is looking for a study coordinator to conduct clinical research while promoting good clinical practice
- •Conducting recruitment, screening, treatment, and follow-up visits with patients per clinical trial protocol requirements
- •Medical chart review, clinical procedures (i.e
- •EKG, spirometry, skin testing, phlebotomy, specimen collection and processing), data review and entry, medication administration and accountability, patient education, administration of questionnaires, and completion of source documentation
- •Learning of numerous clinical trial protocols
- •Communication with patients, sponsors, and all other vendors associated with a clinical trial
- •Resolving data entry queries
- •Participating in monitoring visits
- •Occasional travel out of state for investigator meetings
- •Preparing for and participating in sponsor and federal audits
- •Completing, reviewing, and maintaining regulatory documents
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