Welcome to AbbVie, where we are committed to developing innovative solutions to improve the lives of patients around the world. As a Clinical Research Associate, you will have the opportunity to play a critical role in the development and execution of clinical trials for our cutting-edge pharmaceutical products. We are seeking a highly motivated and detail-oriented individual to join our team and help us bring life-changing treatments to those who need them most. If you have a passion for clinical research, a strong understanding of FDA regulations, and a desire to make a difference, we want to hear from you. Join us at AbbVie and be a part of our mission to make a lasting impact on healthcare.
- Conduct and oversee clinical trials: As a Clinical Research Associate, you will be responsible for conducting and overseeing clinical trials for AbbVie's pharmaceutical products. This includes designing protocols, recruiting participants, and monitoring the progress of the trials.
- Ensure compliance with FDA regulations: You will be expected to have a strong understanding of FDA regulations and guidelines and ensure that all trials are conducted in compliance with these regulations.
- Maintain accurate and detailed records: It will be your responsibility to maintain accurate and detailed records of all clinical trial activities, including participant data, adverse events, and study progress.
- Collaborate with cross-functional teams: You will work closely with cross-functional teams, including medical professionals, regulatory affairs, and data management, to ensure the successful execution of clinical trials.
- Participate in site visits and audits: As needed, you will participate in site visits and audits to ensure that all sites are following protocol and meeting regulatory requirements.
- Communicate trial progress and results: You will be responsible for communicating trial progress and results to internal stakeholders, as well as external partners and regulatory agencies.
- Identify and mitigate risks: You will be expected to identify potential risks and issues during the clinical trial process and work with the team to develop mitigation plans.
- Stay updated on industry developments: As a Clinical Research Associate, it will be your responsibility to stay updated on industry developments and best practices in clinical research to continuously improve trial processes.
- Uphold ethical standards: You will be expected to uphold the highest ethical standards in all aspects of clinical research, ensuring the safety and well-being of trial participants.
- Contribute to the development of new treatments: As a part of AbbVie's mission to improve the lives of patients, you will have the opportunity to contribute to the development of new and innovative treatments through your work in clinical research.
Bachelor's Degree In A Relevant Science Field Such As Biology, Chemistry, Or Pharmacy.
At Least 2-3 Years Of Experience In Clinical Research, Preferably In A Pharmaceutical Or Biotech Company.
Strong Knowledge Of Fda Regulations And Ich Gcp Guidelines.
Excellent Communication And Organizational Skills To Effectively Manage And Coordinate Multiple Clinical Trial Sites.
Ability To Travel Up To 50% Of The Time To Various Clinical Trial Sites And Attend Conferences And Meetings As Needed.
Data Analysis
Regulatory compliance
Clinical Trials
Patient Recruitment
Protocol Management
Study Coordination
Safety Reporting
Informed
Site Monitoring
Investigator Meetings
Good Clinical Practice (GCP)
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Attention to detail
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Research Associate in New York, NY, USA is $72,000 - $97,000 per year. This can vary depending on factors such as experience, education, and the specific company or organization the individual is working for.
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AbbVie is an American publicly traded biopharmaceutical company founded in 2013. It originated as a spin-off of Abbott Laboratories.

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