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Clinical Research Associate - Medical Device

Company

Meridian Bioscience, Inc.
Address , Remote
Employment type FULL_TIME
Salary
Expires 2023-07-01
Posted at 1 year ago
Job Description
About Meridian:
Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems.
Job Summary:
The Clinical Research Associate assists in the administrative of clinical research projects including development of key study documents, oversite of the clinical trial, and ensuring the quality and integrity of the data according to GCP, ICH and SOPs.
Key Duties:
  • Monitor case report forms and electronic data for quality, completeness, and accuracy
  • Assist in the identification and qualification of study sites
  • Keep current on applicable scientific literature.
  • Interact with staff from all departments.
  • Assist in execution of laboratory studies and provide support for clinical trials for new products as needed.
  • Interact with data management and study sites with generation and reconciliation of queries in order to meet business timelines
  • Monitor study sites (site initation visit, intermim monitoring visits and close-out visits) as needed
  • Participates in and adhere to the Quality Program as defined by the QSR Adhere to safety SOPs and report potential safety hazards.
  • Other duties as assigned.
  • Assist with the creation and collection of required study documents both internally and with the investigational study sites
  • Provide answers to common protocol study related questions under the supervison of the Clinical Director or Associate Trial Manager
Qualifications:
Education/Experience:
  • Minimum of 3 years experience as a CRA
  • A. or B.S. in Biological/Health Sciences
  • Preferred: minimum of one year research and development experience

Skills, Specialized Knowledge and Abilities:
  • Excellent written and oral communication
  • Must possess exceptional communication (written and verbal), interpersonal, problem solving and customer service skills.
  • Able to manage workload and priorities
  • Ability to read, understand and follow all company SOPs and guidelines and ensures compliance in direct reports.
  • Willing to travel
  • Strong problem solving abilities.
  • Be a self-starter, detail oriented, organized and able to prioritize and balance workloads and meet strict critical deadlines along with performing under pressure in a fast- paced environment.
  • Strong attention to detail
  • May be required to work additional hours outside of the normal work shift to ensure business commitments are met (evenings and weekends).
  • Basic knowledge in the areas of microbiology, immunology or molecular biology and biochemistry as related to infectious diseases
  • Highly motivated, readily adapts to changing priorities, effectively manages own time to ensure tasks, multiple projects are completed on time.
  • Ability to maintain regular attendance and punctuality requirements.
  • Able to work successfully under tight timelines
  • Computer proficiency with Miscrosoft Office projects

Requirements (Physical, Mental, Environmental Demands):
  • Will be required to be fully gowned for performing tasks in a clean room environment
  • Must be able to wear personal protective equipment (latex or nitrile gloves, face shields/safety glasses, etc.).
  • Must be able to identify and differentiate color on diagnostic devices or components.
  • Must be able to adhere to applicable biosafety practices when on the manufacturing floor or in laboratories
  • Ability to stand, stoop, reach, push and pull throughout the course of the work shift
  • Ability to walk up and down several flights of stairs throughout the work day in a multi-location facility.
  • Must be able to concentrate, analyze and solve complex issues throughout the course of the work shift.
  • Experiments may involve materials that are considered potentially biohazardous. Must be able to work with human substances such as blood, urine, mucus, stool etc.
  • Must have the ability to lift up to 20 pounds of supplies or finished product throughout the work shift.

We are proud to be an EEO/AA employer Minority/Female/Disability/Veteran. We maintain a drug-free workplace and perform pre-employment substance abuse testing.