Clinical Research Assistant (3032) - Clinical Research
Tidewater Physicians Multispecialty Group
Behavioral Health Market Context
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Job Description
xibility as determined after onboarding and training are complete.
Position Summary
Clinical Research Assistant will report directly to the Clinical Research Coordinator and be responsible for performing assigned duties, to include, but not limited to, data mining, data entry and presentation. Candidates with experience working in a research setting are a plus, but not required. A knowledge of medical terminology is helpful.
Major Duties and Responsibilities
• Assess eligibility of potential subjects through review of medical records and discussion of patient status with the Medical Director, the Principal Investigator, other Investigators, nurses and/or the CRC as appropriate.
• Collect, maintain and enter data in keeping with the requirements of the department and the particular study as required; this may be electronic or printed based on requirements of the study.
• Assist the CRC in the performance of other study related duties and general office support as instructed.
• Other duties as assigned.
Knowledge, Skills and Abilities
• Knowledge of medical terminology to include symptomology, diagnoses, medications, anatomy and standard medical equipment and procedures is helpful, but not required.
• Ability to work scheduled hours as defined in the job offer. Must be able to work flexible hours
• Must have excellent interpersonal skills with staff and all health care professionals with excellent verbal and written communication skills, consistent professional conduct, and meticulous attention to detail.
• Must become familiar with the Clinical Research department’s SOP’s and study protocols, and is responsible for following these.
EDUCATION/TRAINING/REQUIREMENTS
• Experience in healthcare preferred.
• Experience with EHR preferred.
• Previous experience with clinical trials a plus.
PHYSICAL DEMANDS
• Ability to stand and walk for long periods of time.
• Ability to sit for extended periods of time.
• Ability to grasp and hold up to 25 lbs.*
• Ability to hear normal voice level communications in person or through the telephone.
• Ability to speak clearly and understandably.
SUCCESS FACTORS
• Excellent Time Management/Organized
• Open Communication/Positive
• Goal Driven
• Excellent Customer Service
• Juggles Multiple Priorities
• Accuracy and Attention to Detail
• Accomplished in word processing and worksheet utilization
Come join the TPMG team!
TPMG is an equal opportunity employer committed to a diverse and inclusive workforce.
Position Summary
Clinical Research Assistant will report directly to the Clinical Research Coordinator and be responsible for performing assigned duties, to include, but not limited to, data mining, data entry and presentation. Candidates with experience working in a research setting are a plus, but not required. A knowledge of medical terminology is helpful.
Major Duties and Responsibilities
• Assess eligibility of potential subjects through review of medical records and discussion of patient status with the Medical Director, the Principal Investigator, other Investigators, nurses and/or the CRC as appropriate.
• Collect, maintain and enter data in keeping with the requirements of the department and the particular study as required; this may be electronic or printed based on requirements of the study.
• Assist the CRC in the performance of other study related duties and general office support as instructed.
• Other duties as assigned.
Knowledge, Skills and Abilities
• Knowledge of medical terminology to include symptomology, diagnoses, medications, anatomy and standard medical equipment and procedures is helpful, but not required.
• Ability to work scheduled hours as defined in the job offer. Must be able to work flexible hours
• Must have excellent interpersonal skills with staff and all health care professionals with excellent verbal and written communication skills, consistent professional conduct, and meticulous attention to detail.
• Must become familiar with the Clinical Research department’s SOP’s and study protocols, and is responsible for following these.
EDUCATION/TRAINING/REQUIREMENTS
• Experience in healthcare preferred.
• Experience with EHR preferred.
• Previous experience with clinical trials a plus.
PHYSICAL DEMANDS
• Ability to stand and walk for long periods of time.
• Ability to sit for extended periods of time.
• Ability to grasp and hold up to 25 lbs.*
• Ability to hear normal voice level communications in person or through the telephone.
• Ability to speak clearly and understandably.
SUCCESS FACTORS
• Excellent Time Management/Organized
• Open Communication/Positive
• Goal Driven
• Excellent Customer Service
• Juggles Multiple Priorities
• Accuracy and Attention to Detail
• Accomplished in word processing and worksheet utilization
Come join the TPMG team!
TPMG is an equal opportunity employer committed to a diverse and inclusive workforce.
Qualifications
- •A knowledge of medical terminology is helpful
- •Knowledge of medical terminology to include symptomology, diagnoses, medications, anatomy and standard medical equipment and procedures is helpful, but not required
- •Ability to work scheduled hours as defined in the job offer
- •Must be able to work flexible hours
- •Must have excellent interpersonal skills with staff and all health care professionals with excellent verbal and written communication skills, consistent professional conduct, and meticulous attention to detail
- •Must become familiar with the Clinical Research department’s SOP’s and study protocols, and is responsible for following these
- •Ability to stand and walk for long periods of time
- •Ability to sit for extended periods of time
- •Ability to grasp and hold up to 25 lbs.*
- •Ability to hear normal voice level communications in person or through the telephone
- •Ability to speak clearly and understandably
- •Open Communication/Positive
- •Excellent Customer Service
- •Juggles Multiple Priorities
- •Accuracy and Attention to Detail
- •Accomplished in word processing and worksheet utilization
Benefits
Responsibilities
- •Clinical Research Assistant will report directly to the Clinical Research Coordinator and be responsible for performing assigned duties, to include, but not limited to, data mining, data entry and presentation
- •Assess eligibility of potential subjects through review of medical records and discussion of patient status with the Medical Director, the Principal Investigator, other Investigators, nurses and/or the CRC as appropriate
- •Collect, maintain and enter data in keeping with the requirements of the department and the particular study as required; this may be electronic or printed based on requirements of the study
- •Assist the CRC in the performance of other study related duties and general office support as instructed
- •Other duties as assigned
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