Novo Nordisk

Clinical Research Associate

Novo Nordisk

Clayton, NC, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Welcome to Novo Nordisk, a global healthcare company dedicated to improving the lives of millions of people worldwide. We are currently seeking a highly motivated and detail-oriented individual to join our team as a Clinical Research Associate. In this role, you will play a vital part in the development of new and innovative treatments for patients with chronic diseases. As a CRA at Novo Nordisk, you will have the opportunity to work with a diverse and collaborative team, while utilizing your skills and expertise to make a meaningful impact on the lives of patients. Our ideal candidate is someone who is passionate about clinical research and has a strong background in the field. If you are looking for a challenging and fulfilling career, we encourage you to apply for this exciting opportunity at Novo Nordisk.

  1. Conduct and oversee clinical trials in accordance with company protocols and industry standards.
  2. Monitor and track study progress, ensuring adherence to timelines and budget.
  3. Collaborate with cross-functional teams to plan and execute clinical trials.
  4. Participate in the development and review of study protocols, informed consent forms, and other study-related documents.
  5. Ensure compliance with regulatory requirements and ethical standards.
  6. Perform site selection, initiation, monitoring, and close-out visits.
  7. Collect, review, and analyze study data for accuracy and completeness.
  8. Communicate with study sites, investigators, and vendors to ensure study progress and data quality.
  9. Identify and resolve study issues in a timely manner.
  10. Assist in the preparation and submission of study reports to regulatory agencies.
  11. Train and mentor new team members on clinical trial processes and procedures.
  12. Attend and present at investigator meetings, study team meetings, and other relevant meetings.
  13. Keep abreast of industry developments and best practices in clinical research.
  14. Maintain accurate and up-to-date study documentation and files.
  15. Adhere to Novo Nordisk's code of conduct and ethical standards at all times.
Where is this job?
This job is located at Clayton, NC, USA
Job Qualifications
  • Bachelor's Or Master's Degree In A Relevant Field Such As Life Sciences, Pharmacy, Or Medicine.

  • Minimum Of 2 Years Of Experience As A Clinical Research Associate In The Pharmaceutical Industry.

  • Strong Knowledge Of Ich-Gcp Guidelines And Other Relevant Regulations And Guidelines.

  • Excellent Communication And Interpersonal Skills To Effectively Collaborate With Cross-Functional Teams And External Stakeholders.

  • Ability To Manage Multiple Tasks And Prioritize Effectively In A Fast-Paced And Dynamic Environment.

Required Skills
  • Quality Assurance

  • Data Management

  • Regulatory compliance

  • Study Coordination

  • Protocol Adherence

  • Site Monitoring

  • Adverse Event Reporting

  • Subject Recruitment

  • Investigator Training

  • Gcp Knowledge

  • Protocol Deviation Management

Soft Skills
  • Communication

  • Conflict Resolution

  • Emotional Intelligence

  • Leadership

  • Time management

  • creativity

  • Critical thinking

  • Teamwork

  • Adaptability

  • Problem-Solving

Compensation

According to JobzMall, the average salary range for a Clinical Research Associate in Clayton, NC, USA is $60,000-$90,000 per year.

Additional Information
Novo Nordisk is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedMarch 29th, 2024
Apply BeforeMay 22nd, 2025
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About Novo Nordisk

Novo Nordisk AS engages in the research, development, manufacture, and marketing of pharmaceutical products. It operates through the Diabetes and Obesity Care; and Biopharmaceuticals segments. The Diabetes and Obesity Care segment covers insulins, glucagon-like-peptide 1, other protein-related products, oral anti-diabetic drugs and obesity. The Biopharmaceuticals segment handles the research, development, manufacture, and distribution of products within the areas of haemophilia, growth hormone, hormone replacement, inflammation and other therapy areas.

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