Welcome to Beckman Coulter, a leading medical technology company that strives to improve healthcare worldwide. We are currently seeking a highly experienced Senior Clinical Research Associate to join our dynamic team. As a Senior CRA, you will play a crucial role in managing and monitoring clinical trials to ensure the safety and efficacy of our cutting-edge products. We are looking for a dedicated and detail-oriented individual who has a strong background in clinical research and a passion for making a positive impact in the healthcare industry. If you have the qualifications and drive to excel in this role, we encourage you to apply and be a part of our mission to transform healthcare.
Manage and monitor clinical trials to ensure compliance with protocols, regulations, and timelines.
Conduct site visits to ensure proper documentation and adherence to study procedures.
Work closely with cross-functional teams to develop and implement clinical trial plans.
Review and analyze clinical data to identify any potential risks or issues.
Collaborate with investigators and study coordinators to ensure participant safety and data integrity.
Train and mentor junior clinical research associates.
Maintain accurate and timely documentation of all study activities.
Communicate study progress and updates to project teams and management.
Identify and address any deviations from study protocols.
Maintain knowledge of industry regulations and guidelines.
Participate in study start-up activities, including site selection and initiation visits.
Ensure proper storage and handling of investigational products.
Assist in the development of study protocols and other study-related documents.
Attend investigator meetings and provide updates on study progress.
Maintain confidentiality of all study data and information.
Contribute to continuous improvement efforts within the clinical research department.
Act as a liaison between study sites and the company.
Proactively identify and communicate potential risks or issues that may impact study timelines or outcomes.
Assist in the preparation of study reports and presentations.
Uphold the company’s mission and values while representing Beckman Coulter in a professional and positive manner.
Where is this job?
This job is located at Chaska, MN 55318, USA
Job Qualifications
Bachelor’s Degree In A Relevant Field Such As Life Sciences, Pharmacy, Or Medicine.
Minimum Of 5 Years Of Experience As A Clinical Research Associate, Preferably In A Senior Role.
Strong Knowledge Of Good Clinical Practice (Gcp) Guidelines And Relevant Regulations.
Proven Experience In Managing And Monitoring Clinical Trials, Including Site Selection, Initiation, And Close-Out Activities.
Excellent Communication And Organizational Skills, With The Ability To Work Independently And As Part Of A Team.
Required Skills
Quality Assurance
Data Analysis
Budget Management
Regulatory Compliance
Site Management
Clinical Trials
Patient Recruitment
Protocol Development
Investigator Meetings
Medical Device Expertise
Electronic Data Capture
Soft Skills
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Problem Solving
Time Management
Interpersonal Skills
Creativity
Teamwork
Adaptability
