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Form of workJob 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
Clinical Research Coordinator 1 Position Description
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 AMRs 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 studys 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.
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.
** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.
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
Clinical Research Coordinator 1 Position Description
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 AMRs 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 studys 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.
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.
** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.
