Research Assistant I - Clinical Research
Behavioral Health Market Context
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Benefits
Health Insurance
Job Description
nts, lab kits, and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection.
• Communicating with study participants, caregivers, third-party vendors, and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Requirements
• Interest in and knowledge of specific study indications.
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
• Strong personal initiative and attention to detail.
• Ability to react calmly and effectively in emergency situations.
• Ability to interpret, adapt and apply guidelines and procedures.
• Ability to clearly communicate both orally and verbally.
Benefits
• Health Insurance
• Dental
• Vision
• LTD
• STD
• Life Ins
• 401k
• Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection.
• Communicating with study participants, caregivers, third-party vendors, and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Requirements
• Interest in and knowledge of specific study indications.
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
• Strong personal initiative and attention to detail.
• Ability to react calmly and effectively in emergency situations.
• Ability to interpret, adapt and apply guidelines and procedures.
• Ability to clearly communicate both orally and verbally.
Benefits
• Health Insurance
• Dental
• Vision
• LTD
• STD
• Life Ins
• 401k
Qualifications
- •Interest in and knowledge of specific study indications
- •Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.)
- •Skilled in organization and record maintenance
- •Skilled in developing and maintaining effective working relationships with supervisors and co- workers
- •Strong personal initiative and attention to detail
- •Ability to react calmly and effectively in emergency situations
- •Ability to interpret, adapt and apply guidelines and procedures
- •Ability to clearly communicate both orally and verbally
Benefits
- •Health Insurance
- •Dental
- •Vision
- •LTD
- •STD
- •Life Ins
- •401k
Responsibilities
- •Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies
- •Creating and maintaining patient charts for all assigned studies
- •Preparing participant visits based on CRC's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate
- •Filing of lab results, EKG results, and other communication in designated patient charts
- •Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials
- •Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication
- •Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection
- •Communicating with study participants, caregivers, third-party vendors, and laboratories as needed
- •Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks
- •Aiding Coordinators in the facilitation of study monitoring visits
- •Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants
- •Assumes other duties and responsibilities as assigned
- •The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive
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