Clinical Research Coordinator

2110 East Flamingo Road, Las Vegas, United States

Alliance for Multispecialty Research

Posted on: September 2, 2020

Closing: October 02, 2020

Salary: Undisclosed

Position Type: Full Time

Job Description

The Clinical Research Coordinator I will perform multiple and varied tasks critical to the management of clinical research studies.  The Clinical Research Coordinator I is expected to exhibit basic knowledge of clinical research activities and adhere to federal and other applicable regulations.  The Clinical Research Coordinator I must ensure compliance with protocol guidelines, identify problems and/or inconsistencies and monitor subject process throughout the clinical research study.

 

To consistently embody AMR’s Core Values:

  • Excellence and Consistency
  • Collaborative Innovation
  • Respect for our Subjects, Sponsors and Team Members
  • Community
  • Unimpeachable Ethics

The Clinical Research Coordinator reports to the Clinical Operations Manager.

Classification: Non-Exempt

Salary based on experience level

Primary Responsibilities:

  • Communicates effectively and courteously with study patients.
  • Acknowledges study patients' needs and tends to them appropriately.
  • Knowledge of current studies being conducted
  • Collects patient medical history and conditions.
  • Obtain Informed Consent.
  • Maintains site regulatory files and study documents.
  • Study drug dispense and accountability.
  • Collect and evaluate concomitant medication.
  • Collect and evaluate medical records for compliance.
  • Assist in data collection for A/E and SAE assessments.
  • Perform EKG, vital signs, and protocol-specific procedures.
  • Collect and process blood, urine, and tissue samples.
  • Review clinical blood lab reports for protocols compliance and safety.
  • Verify the accuracy of data collected.
  • Document temperatures for IP stored on-site.
  • Recruit study patients by calling subjects from the database.
  • Participate in offsite recruitment events as needed.
  • QC study e-source to comply with the study protocol.
  • Manage all required study startup documentation, training, and timelines on assigned study protocols.
  • Other tasks and responsibilities as requested to facilitate business needs.
  • Comprehensive knowledge of company's SOPs, policies and Confidentiality agreements
  • Knowledge of safety hazards and procedures that establish a safe work environment
  • Other tasks and responsibilities as requested to facilitate business needs.

Desired Skills and Qualifications:

  • 2+ years of CRC research experience (Required)
  • Accredited medical assistant certificate and/or laboratory assistant certificate
  • CPR and first aid certification (Preferred)
  • IATA and/or Safe-T-Pak certification for shipment lab specimens and/or dry ice (Preferred)
  • GCP and protection of Human Subject Participants (Preferred)
  • Skilled in computer and data collection software
  • Phlebotomy, EKG, and other technical skills as required per protocol
  • Comprehensive knowledge of FDA, GCP, and HIPAA as applicable to clinical research
  • Ability to multi-task and perform multiple critical tasks simultaneously (under dynamic and ever-changing conditions and deadlines).
  • Exceptional written and verbal communication skills.
  • Ability to work independently, lead clinical research studies and complete tasks.
  • Calm, friendly, approachable, and presents a professional image.
  • Excellent listening, written, and verbal communication skills.
  • Committed, highly energetic, self- motivated and highly organized.
  • Demonstrated proficiency in office equipment including (but not limited to) copy machines, facsimile machine, multi-line telephones and computers.
  • Proficient in Microsoft Office products including Outlook, Word, and Excel.
  • Professional and highly motivated “self-starter” with the ability to exercise initiative.
  • Excellent task management and prioritization skills.

 

Alliance of Multispecialty Research does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.

Alliance for Multispecialty Research

Posted on: September 2, 2020

Closing: October 02, 2020

Salary($): Undisclosed

Position Type: Full Time

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