Medical Assistant Job at SQRL, Euless, TX

MzlEQTZpOWFHckxXaFpyWDJYMDgwZEx5eGc9PQ==
  • SQRL
  • Euless, TX

Job Description

Highlights

  • Play a key role in helping patients get involved in clinical trials
  • up to $18 - $24 an hour+ full benefits
  • Monday - Friday; no weekends!
  • Growth opportunities to CRC, Sr. CRC, and more!
  • Great stepping stone into research, or a way to get more experience!

As an entry-level Clinical Research Medical Assistant, you will be integral to the success of our research endeavors, providing essential support throughout all phases of clinical trials. Key responsibilities include:

  • Assist in Start-up and Implementation Activities: Collaborate with the research team to facilitate the initiation of new studies, including protocol development and regulatory submissions.
  • Completion and Submission of Clinical Trials Amendments: Ensure timely completion and accurate submission of all amendments to the Institutional Review Board (IRB), adhering to regulatory guidelines and protocols.
  • Editing Informed Consent Documents: Review and edit informed consent documents to ensure clarity, accuracy, and compliance with regulatory standards.
  • Correspondence with Stakeholders: Serve as a primary point of contact for communication with the IRB, investigators, and sponsors throughout the clinical trial process, maintaining open lines of communication and addressing inquiries promptly.
  • Preparation of Annual Progress Reports: Compile and prepare comprehensive progress reports for IRB renewal of ongoing studies, summarizing key findings and milestones achieved.
  • Collection and Submission of Regulatory Documents: Facilitate the collection, completion, and submission of regulatory documents to various regulatory entities, ensuring compliance with regulatory requirements.
  • Maintenance of Regulatory Binders: Establish and maintain regulatory binders and other relevant files, organizing documentation meticulously during the review, approval, and activation process for clinical trials.
  • Coordination of Safety Reports: Coordinate the review and processing of safety reports to the IRB, ensuring prompt reporting and appropriate follow-up actions as required.

Qualifications:

  • Bachelor's degree in a relevant field (e.g., life sciences, healthcare administration, or related discipline) preferred.
  • Certified Medical Assistant Certification preferred
  • Prior experience in clinical research or healthcare administration is preferred.
  • Experience with Phlebotomy, EKG, taking Vitals, etc. REQUIRED
  • Strong attention to detail and organizational skills.
  • Excellent written and verbal communication abilities.
  • Familiarity with regulatory requirements governing clinical research (e.g., FDA regulations, ICH-GCP guidelines) is desirable.

Job Tags

Monday to Friday,

Similar Jobs

Maania Consultancy Services

SAP Hybris Architect/Lead/Consultant Job at Maania Consultancy Services

 ...Client is looking for a Hybris Application Architect Managing Consultant. The candidate will lead Hybris project team members in the design...  ...3 years of experience in integrating commerce solutions with SAP Enterprise Resource Planning (ERP) applicationsAt least 5 years... 

TEKsystems

React JS Developer Job at TEKsystems

 ...Job Description Job Description Currently looking for a Senior UI Developer who specializes in React and can help support critical channels in different lines of business for an exclusive position with one of our Major Enterprise clients. Ideal candidates must have... 

Wind River

Key Account Manager Job at Wind River

 ...hat require the highest levels of security, safety, and reliability. Wind River helps customers across automotive, aerospace, defense, industrial, medical, and telecommunications industries solve complex technology challenges on their jour... 

Syneos Health

Medical Science Liaison Job at Syneos Health

 ...educator and a gifted cultivator of new and exciting opportunities grounded in science.In this role, you will confer with internal stakeholders and build new collaborative relationships with medical and scientific leaders, policymakers, and advocates. Youll contribute... 

Dexcom

Sr Director Global Commercial Strategy Job at Dexcom

 ...Acquisition at ****@*****.***.View the OFCCP's Pay Transparency Non Discrimination Provision at this link .Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click...