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Overnight Trial Master File Jobs in Georgia (NOW HIRING)

Syneos Health

CRC II (Onsite) - Marietta, GA

Marietta, GA · On-site

$23 - $30.50/hr

Prepare and maintain the Investigator Site File and/ or Trial Master File (TMF) for the study. * Participate in creation and review of timelines and start-up meetings (Investigator Meeting/SIV ...

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA

$71K - $145K/yr

During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the ...

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA · On-site

$71K - $145K/yr

During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the ...

Tucker Ellis LLP

Litigation Paralegal

Atlanta, GA · On-site

Finalize court filings, ensuring accurate citations; verifying compliance with local rules ... Prepare exhibits for motions, hearings, depositions, and trial by labeling, combining, organizing ...

Tucker Ellis LLP

Litigation Paralegal

Atlanta, GA · On-site

Finalize court filings, ensuring accurate citations; verifying compliance with local rules ... Prepare exhibits for motions, hearings, depositions, and trial by labeling, combining, organizing ...

Robert Half

Staff Accountant

Savannah, GA · On-site

$24 - $28/hr

Review master data records and recommend updates that improve the accuracy and consistency of ... Assemble documentation and schedules required for annual filings such as sales tax reports, 1099s ...

Fox Rothschild

Legal Team Assistant

Atlanta, GA

... i.e., trial exhibits); * Scan and process third party vendor invoices; * Process attorneys ... overnight/mail service deliveries; * Create and maintain original and electronic client case files ...

Danaher

Principal Clinical Scientist

Atlanta, GA · On-site +1

This role is responsible for clinical trial strategies within the US and EU regions for Danaher ... Author and review clinical and regulatory documentation-including study reports, technical files ...

Department of Justice

Paralegal Specialist

Macon, GA · On-site

$61K/yr

OR a Master's or equivalent graduate degree or higher; OR 2 full years of progressively higher ... files to identify relevant issues and potential evidence; conducting legal research concerning ...

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Clinical Research Associate (CRA) -Cardiovascular Medical Device

Marietta, GA • On-site

Mirus LLC
1 - 10 employees
Learn more about Mirus LLCexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 days ago

Job description


Role: Clinical Research Associate (CRA) - Cardiovascular Medical Device 

Location: Remote  

Position Summary: 

Assist with the management of cardiovascular clinical studies for MiRus products with a focus on adherence to critical timelines, high-caliber document development and quality data collection. The applicant should possess strong critical thinking skills and the ability to comprehend technical subject matter to effectively contribute to the organization.

Essential Duties and Responsibilities:
 

  • Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents.
  • Assist with the management of investigational studies from start through study closure.
  • Engage in new study trial design with cross functional teams, including clinical and pre-clinical research and development groups.
  • Contribute to the development of CRFs
  • Assist with the formulation of instructional materials and training of investigators, study coordinators and associated study site personnel on the conduct of the clinical trials, as applicable.
  • Assist Study Manager with safety monitoring including preparing supporting documentation for CEC and/or DSMB, meetings, agenda, data review, presentations, and updating relevant trackers as applicable.
  • Serve as a point of contact between clinical site investigators and the MiRus team.
  • Work with investigators and site personnel to quickly and effectively resolve discrepancies.
  • May be responsible for patient accruals and tracking payments to sites for clinical study programs
  • Serve as a point of contact between CRO personnel and MiRus.
  • Oversee/support CRO and field study monitors, with monitoring related items and follow-up on study tasks.
  • Monitor ongoing compliance to study protocols in accordance with applicable regulations and GCP, work instructions, guidelines and/or policies.
  • Provide continuous data review of source documents, case report forms, data reports as appropriate.
  • Assist in review of monitoring reports and tracking of action items.
  • Review source documentation to confirm subject eligibility for clinical trials.
  • Track and upload study imaging
  • Manage clinical study documentation (trial master file and study related tracking).
  • Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager
  • Interact with data management, as applicable
  • Support applications and technical files as needed.
  • Assist with preparation for investigators meetings.

 Minimum Education and/or Experience: 

  • Bachelor’s or Master’s degree in nursing with clinical experience in the cardiac field (CCU, CVOR, Cath Lab) and experience in a clinical research role.  CRA certification desired.
  • At least 2 years of experience in clinical research role, with at least 2 years in CRA role, preferably in cardiovascular medical device.
  • Experience in clinical trials and/or post-market registries in the U.S., Australian and/or European Union, with other geographies desired.
  • Current knowledge of medical device clinical trials design and best practices.
  • Proficient knowledge of FDA regulations and ICH/GCP guidelines, guidance documents, and other applicable regulations and standards, and implementation of these standards in the medical device industry, in the U.S. and all countries in which trials are conducted.
  • General application of medical terminology (cardiovascular specific preferred).

 Benefits:
MiRus offers competitive compensation, options, full benefits, and relocation assistance.

  •  401(k)
  •  Dental insurance
  • Vision insurance
  •  Disability insurance
  •  Employee assistance program
  •  Flexible spending account or Health Savings Account
  •  Health insurance
  •  Life insurance
  •  Paid time off

 Schedule:

  • Monday to Friday (8am – 5pm)

Work Location:

  • Remote
  • Position may require domestic travel at least 20-40%

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