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Arkansas Dermatology · 1 week ago

Clinic Research Coordinator

North Little Rock, AR

Full-time

Onsite

Entry Level

1+ years exp

Arkansas Dermatology is committed to providing the highest level of expertise in dermatologic care. They are seeking a Clinic Research Coordinator to lead patient recruitment for clinical trials, assist in regulatory affairs, and ensure compliance with clinical research protocols.

Health CareMedicalService Industry

Responsibilities

Lead research recruitment by calling and scheduling patients for screening and enrollment visits with dermatology patients

Assist Directors of Clinical Research and Regulatory Affairs to develop, implement, and maintain internal documents, workflows, processes, procedures, and systems

Performs protocol-specific clinical tasks including assessment, screening, ordering tests, collecting specimens, and monitoring responses to the investigational treatment

Assist in maintaining legal documents and government reporting regulations affecting human resource functions such as OSHA, ADA, and HIPAA

Acts as an expert consultant to investigators to ensure Good Clinical Practice (GCP) standards and Standard Operating Procedures (SOPs) are followed

Maintain and create regulatory binders for clinical trials. Maintaining filing for all documents and binders

Create and develop source documentation for clinical trials

Lead by example, maintain positive team morale, and create an exceptional organizational culture

Qualification

Clinical research experienceClinical Practice (GCP)Regulatory complianceMicrosoft Word/ExcelDatabase managementDependabilityHard-workingSchedulingTeachTeam-building skillsEthical mindsetAutonomous workOrganizational skillsVerbal communicationWritten communicationInterpersonal skillsCalm under pressureSelf-starterProblem-solvingConflict resolution

Required

Minimum required experience in clinical research: 1 year

Lead research recruitment by calling and scheduling patients for screening and enrollment visits with dermatology patients

Assist Directors of Clinical Research and Regulatory Affairs to develop, implement, and maintain internal documents, workflows, processes, procedures, and systems

Performs protocol-specific clinical tasks including assessment, screening, ordering tests, collecting specimens, and monitoring responses to the investigational treatment

Assist in maintaining legal documents and government reporting regulations affecting human resource functions such as OSHA, ADA, and HIPAA

Acts as an expert consultant to investigators to ensure Good Clinical Practice (GCP) standards and Standard Operating Procedures (SOPs) are followed

Maintain and create regulatory binders for clinical trials. Maintaining filing for all documents and binders

Create and develop source documentation for clinical trials

Lead by example, maintain positive team morale, and create an exceptional organizational culture

Dependability

Hard-working

Competent with Microsoft Word/Excel and Google Calendar

Excellent organizational skills and attention to detail

Scheduling

Ability to teach

Exceptional verbal and written communication skills

Excellent interpersonal skills with the ability to manage sensitive and confidential situations with tact, professionalism, and diplomacy

Team-building skills and high emotional intelligence

Ethical mindset

Able to work autonomously

Remain calm under pressure

Self-starter and proactive tendencies

A commitment to partner with leadership to drive a culture where every employee is a problem-solver, working together to identify and correct problems that impact the patient experience

Adept to problem-solving, delegating, negotiating, and conflict resolution

Experience with computer data entry and database management