Research Assistant Job at AMR Clinical, Wichita, KS

Q2ZLV0J3Unh5Zmx0NFNndTRCRkw0SWNKa0E9PQ==
  • AMR Clinical
  • Wichita, KS

Job Description

The role of the Research Assistant is responsible for performing a wide variety of administrative and clinical tasks to support the study site. The Research Assistant supports all study related activities to ensure that the study is completed accurately per study protocol. The Research Assistant is an integral role to assist with the flow of the clinic. 

 

To consistently embody AMR Clinical’s Core Values:

  • United We Achieve
  • Celebrate Diverse Perspectives
  • Do the Right Thing
  • Adapt and Persevere

The Research Assistant reports to the Site Manager/Team Lead.

Classification: Non-Exempt

Primary Responsibilities:

  • Effectively prioritize tasks and meet deadlines in a fast-paced environment.
  • Maintain a strong emphasis on compliance responsibilities, including timely identification and reporting of protocol deviations, serious adverse events (SAEs), and adherence to regulatory and site-specific requirements.
  • Monitor & Report Adverse Events – Recognize and promptly report AEs, protocol deviations, and safety concerns to the clinical team. Document AEs and Serious Adverse Event reporting in compliance with FDA, IRB, and sponsor requirements, ensuring timely follow-up and resolution.
  • Ensure Compliance with Study Protocols & Regulatory Guidelines – Adhere to Good Clinical Practice (GCP), FDA regulations, and site SOPs when conducting study-related activities.
  • Assist in Subject Retention Efforts – Support ongoing engagement, communication, and compliance to enhance subject retention throughout the study.
  • Perform Inventory Management – Track and manage study supplies, lab kits, and investigational products (if applicable) to ensure readiness for study visits.
  • Assist in maintaining accurate, timely, and audit-ready documentation of all study-related activities.
  • Perform Laboratory Responsibilities with Accuracy – Ensure proper labeling, handling, storage and shipment of specimens per protocol and regulatory requirements.
  • Strong problem-solving skills and ability to adapt to evolving study requirements.
  • Ability to handle confidential and sensitive information with discretion.
  • Ability to follow detailed instructions and maintain high levels of accuracy.
  • Establish and maintain patient rapport during clinical drug trials to include management of subjects
    1. Clinical data collection such as vital signs, EKG recording, subject weights, etc.
    2. Medical record retrieval and review when required
    3. Subject interviews
    4. Phlebotomy
    5. Filing and pulling study records
    6. Answering and triage of research office calls
    7. Subject check in and out process
  • Study preparation, such as screening packets, preparing informed consents, pulling charts for the next business day, etc.
  • Filing study documents in the subject’s chart.
  • Develop rapport with study sponsors, monitors, study participants, etc. 
  • Assist monitors during onsite visits
  • Maintain accurate enrollment/ICF logs
  • Assist the clinical team to complete study activities. The clinical team includes but is not limited to CRCs, Laboratory, Data management, etc
  • Educate subjects on diaries as studies require. 
  • Accurate and timely documentation
  • Unblinded duties as assigned.
  • Position may require occasional weekend and/or overtime hours. 
  • Other duties as assigned
  •  

Desired Skills and Qualifications:

  • Medical office experience, medical certificate, or equivalent work experience preferred. 
  • Phlebotomy skills are preferred
  • Excellent attention to detail
  • Strong listening, verbal and written communication skills
  • Excellent task management and organizational skills
  • Ability to multi-task in an always evolving fast paced environment. 
  • Demonstrate proficient knowledge of operating office equipment and software. 
  • Ability to be ambulatory most of the workday.
  • Ability to lift/transfer/push/manipulate equipment and patients, which requires strength, gross motor and fine motor coordination.

 

AMR Clinical 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.

Compensation details: 20-23 Hourly Wage

PIdb75d554f34c-30492-38778206

Job Tags

Hourly pay, Work experience placement, Work at office,

Similar Jobs

Blue Star Partners LLC

Training Coordinator Job at Blue Star Partners LLC

 ...Job Title: Training Coordinator Location: Scarborough, ME Onsite Local candidates only Period:09/23/2024 to 12/31/2024 possibility of extension Hours/Week: 40 hours (Hours over 40 will be paid at Time and a Half) Rate:$25-$30/hour Contract... 

The Little Gym International

Special Events Coordinator & Sales Manager Job at The Little Gym International

 ...a ton of fun, you may be the person we are looking for! What We Expect From You Lead/Assist amazing Birthday Parties and special events based on our proven curriculum and teaching method (dont worry, well teach you how!) Manage grassroots community events and... 

Optigy

Endocrinology Opportunity in Birmingham, AL making $320k + Job at Optigy

 ...AM 5:00 PM No nights or weekends Minimal hospital rounding (site dependent) Practice Model Value-Based Outpatient Endocrinology Geriatric-focused patient population Small patient panel1216 patients per day Dedicated support team: Medical Assistant... 

Globe Life AO

Fully Remote - Customer Service Representative - (No Experience Needed) Start ASAP + Bonuses Job at Globe Life AO

HIRING NOW Remote Customer Support Rep Weekly Pay + Training Provided Looking for a remote job with flexible hours, weekly pay, and career growth ? Join Globe Life AO , where we train you from scratch and give you the tools to succeed no experience required!...

St David's Round Rock Medical Center

Staff Registered Nurse New Graduate Job at St David's Round Rock Medical Center

Vivian Concierge is seeking a Registered Nurse (RN) New Graduate for a nursing job in Round Rock, Texas. Job Description & Requirements...  ...is a year-long program designed to give you hands-on experience to help establish valuable clinical and critical thinking skills...