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Alliance for Multispeciality Research, LLC
Kansas, MO | Full Time
$56k-74k (estimate)
2 Months Ago
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Clinical Research Assistant
Apply
$56k-74k (estimate)
Full Time 2 Months Ago
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Alliance for Multispeciality Research, LLC is Hiring a Clinical Research Assistant Near Kansas, MO

Benefits:
  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance
 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 role of the Clinical Research Assistant is to perform a wide variety of clinical and administrative tasks to assist the clinical research coordinator in conducting clinical trials. The research assistant is responsible for study support activities to ensure each study is completed accurately, according to protocol, and on time.
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 Assistant reports to the Team Lead/Site Manager/General Manager.
Classification: Non-Exempt
Primary Responsibilities:
· Assist coordinators with administrative study activities in a timely manner as necessary.
· Assist monitor during all site visits if applicable.
· Maintain accurate enrollment/drug logs if applicable.
· Assist in general office workflow which includes telephone answering.
· Responsible for assisting regulatory administration work for necessary periodic IRB reviews, both ongoing and final.
· Establish and maintain patient rapport during clinical drug trials to include management of subjects
o Clinical data collection such as vital signs, EKG recording, subject weights
o Medical record retrieval and review when required
o Subject interviews
o Phlebotomy
o Specimen collection, processing, and storage
o Complete source documentation
o Filing and pulling study records
o Transporting clinical specimens to the laboratory
o Answering and triage of research office calls
· Work with physicians and other staff to maintain a more effective and systematic method to investigate clinical problems related to the support of the clinical trial patients.
· Facilitate communication between the site and various monitors, to include telephone and written correspondence as well as monitoring visits.
· Scheduling of various visits/procedures
· Assists providers with various visits/procedures
· Perform site and protocol specific training in a timely manner
· Other duties as assigned
Additional Responsibilities (Check If Applicable):
Cross train in lab coordinator duties to serve as a backup.
Monitor patient arrivals and check-in subjects according to receptionist duties
Responsible for filing source documents in the subjects charts
Take patient history
Train subjects on diaries
Create screening charts once the screen source is available
All screening chats and randomization charts for the next day pulled
Clinic rooms and subject bathrooms are stocked including necessary medical supplies
Desired Skills and Qualifications:
· At least 6 months of past medical office experience, medical certificate, or equivalent previous work experience required.
· Phlebotomy skills preferred
· Ability to work consistently and effectively as part of a high-performance work team.
· Ability to effectively devote keen and acute attention to detail.
· Demonstrated ability to exercise standard Universal Precautions, or ability to quickly learn and apply Universal Precautions.
· Positive attitude and the ability and desire to work in a company that embraces collaboration and a team approach.
· Demonstrated ability to operate basic office equipment including (but not limited to) copy machines, facsimile machine and computers.
· Strong verbal and interpersonal skills
· Professional and highly motivated “self-starter” with the ability to exercise initiative, together with ability to work as a team player as well as independently while managing a variety of skills in a variety of software environments, i.e., Word, Excel, Internet.
· Excellent task management and prioritization skills.
· Proven ability to successfully build and cultivate excellent long-term relationships
· Excellent follow up
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.** 

Job Summary

JOB TYPE

Full Time

SALARY

$56k-74k (estimate)

POST DATE

03/05/2023

EXPIRATION DATE

06/15/2024

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The following is the career advancement route for Clinical Research Assistant positions, which can be used as a reference in future career path planning. As a Clinical Research Assistant, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Assistant. You can explore the career advancement for a Clinical Research Assistant below and select your interested title to get hiring information.

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If you are interested in becoming a Clinical Research Assistant, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Clinical Research Assistant for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

Quotes from people on Clinical Research Assistant job description and responsibilities

Certifications are also available for this position through The Society of Clinical Research Associates (SOCRA) and The Association of Clinical Research Professionals.

01/04/2022: Santa Barbara, CA

Analyze and evaluate clinical data gathered during research.

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Provide regular report updates of the progress of clinical studies to the appropriate personnel.

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These clinical trials are very much regulated and seriously monitored to ensure that they comply with the laid down regulations.

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Must be able to ensure that data gotten from clinical trials are accurate and reliable and the legal rights and privacy of the subjects are protected.

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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Clinical Research Assistant jobs

Fact-checking, editing, and proofreading research documents for accuracy and consistency.

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Research Assistants provide support to research teams who are conducting experiments or gathering and analysing data.

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Maintained FDA clinical trial documentation for department and received excellent FDA audits of records.

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Have strong customer focus and good communication skills

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For example, clinical research associate candidates should have excellent attention to detail and organizational skills since they’re responsible for monitoring and reporting on the results of clinical trials.

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Step 3: View the best colleges and universities for Clinical Research Assistant.

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