Are you a Medical Assistant looking for a change? Interested in a challenging career where you are involved in the development of pharmaceuticals?
If you answered YES and are looking for a Mon-Fri stable schedule working days, then AMR could be the next step in your career!
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 will perform multiple and varied tasks critical to the management of clinical research studies. The Clinical Research Coordinator is expected to exhibit basic knowledge of clinical research activities and adhere to federal and other applicable regulations. The Clinical Research Coordinator 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 Site Manager.
Classification: Non-Exempt
Primary Responsibilities:
- Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
- Intermediate knowledge of SOPs and ensure they are adhered to in the conduct of the clinical research study.
- Intermediate 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, 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.
- Serve as a preceptor and assist in training of research staff as needed.
- Possess a willingness to assume responsibility for tasks outside of your current role and to work flexible hours as needed.
- Other duties as assigned
Additional Responsibilities:
- Participate in study start-up activities, such as supply inventory and regulatory documentation.
- Track status of study participants (e.g, randomized, screen failed, etc)
- Schedule participant visits according to protocol-specified visit windows.
- Document protocol deviations
- Ensure all data points are collected at each study visit
- Coordinate research staff to assist with study visits
- Anything printed on thermal paper (ECGs, bladder scan results) MUST be photocopied. Stamp the copy with the “certified copy” stamp and initial/date. Attach original document to certified copy before filing in the patient’s chart. Note: One printout will go in the source charts while the second original is out for review and signature. Once the MD signs, the signed original with the certified copy is filed in the source chart. The second printout is removed and shredded.
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.
- At least one year of clinical experience and at least one year research experience required.
- Proficient as a Clinical Research Coordinator 1.
- Ability to interpret and perform clinical, laboratory and diagnostic tests (such as vital signs, height, weight, temperature, etc.).
- 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, delegation 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.
Job Type: Full-time
Pay: $24.00 - $27.00 per hour
Expected hours: 40 per week
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Employee assistance program
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
- Weekends as needed
Experience:
- Phlebotomy: 2 years (Required)
- Patient care: 2 years (Required)
- Clinical research: 2 years (Preferred)
License/Certification:
- Certified Medical Assistant (Required)
Work Location: In person