Clinical Research Coordinator

Clinical Research Coordinator 1 Position Description

Alliance for Multispecialty Research is a fast-growing clinical research organization that conduct trials for the development of pharmaceuticals.

AMR offers competitive pay, 401K matching, health/dental/vision, paid STD and LTD, as well as on demand access to your pay!

Team Member Benefits:

· Health, Dental, Vision

· Supplemental Life Coverage

· Short-term Disability and Long-term Disability (AMR covers cost)

· Life Insurance (AMR covers cost of AD&D $50,000)

· 401K (employer matching)

· Paid Time Off

· Holiday Pay

· Employee Assistance Program

Position Overview

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

Primary Responsibilities:

· Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.

· Basic understanding of SOPs and ensure they are adhered to in the conduct of the clinical research study.

· Basic understanding of medications per clinical trial.

· Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.

· Effectively communicate with clinical research sponsors, CROs, monitors/CRAs, IRBS, laboratories and clinical personnel within the research industry.

· Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research study.

· Notify Investigator, monitor/CRA of any adverse events or serious adverse events per the protocol.

· Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately.

· Complete all required documentation in a legible and timely fashion.

· Ensure all necessary documents are appropriately signed and dated.

· Possess a willingness to assume responsibility for tasks outside of your current role and to work flexible hours as needed.

Desired Skills and Qualifications:

· Successful completion of a formal medical/clinical educational program or in the alternative has a strong knowledge of medical terminology and the ability to learn quickly.

· Clinical experience involving patient care in a healthcare environment preferred but not required.

· Ability to interpret and perform clinical, laboratory and diagnostic tests (such as vital signs, height, weight, temperature, etc.) preferred.

· Ability to function independently with minimal supervision, and to exercise discretion and a high level of good clinical and other professional judgement.

· 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.

Job Type: Full-time

Pay: $40,000.00 - $55,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Employee assistance program
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Referral program
• Retirement plan
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Education:

• Associate (Required)

Experience:

• Clinical Research: 1 year (Preferred)

Work Location: One location