Experienced Clinical Research Associate, Sponsor Dedicated
Welcome to IQVIA, a leading global provider of advanced analytics, technology solutions, and contract research services to the life sciences industry. We are currently seeking an experienced Clinical Research Associate to join our team as a Sponsor Dedicated CRA. In this role, you will have the opportunity to work directly with our sponsor clients, driving clinical research projects from start to finish and ensuring their success. We are looking for a highly motivated and detail-oriented individual with strong communication skills and a proven track record in clinical research. If you are passionate about making a difference in the healthcare industry and have the required qualifications, we invite you to apply and join our dynamic team at IQVIA.
- Conduct clinical research activities in accordance with applicable regulations, protocols, and company standard operating procedures.
- Serve as the primary point of contact for sponsor clients, maintaining regular communication and providing updates on project progress.
- Develop and maintain relationships with sponsor clients, understanding their needs and ensuring their satisfaction with the services provided.
- Collaborate with cross-functional teams to plan and execute clinical research projects, including study start-up, monitoring, and close-out activities.
- Conduct site selection, initiation, and monitoring visits, ensuring compliance with study protocols and regulatory requirements.
- Monitor and track study progress and data quality, identifying and addressing any issues or risks that may impact the project timeline or data integrity.
- Prepare and review study-related documents, including protocols, informed consent forms, and monitoring reports.
- Train and mentor junior staff members on study protocols, regulations, and company procedures.
- Maintain accurate and timely documentation of all study-related activities and communications.
- Participate in internal and external audits and inspections, providing necessary support and addressing any findings.
- Continuously improve processes and procedures to enhance efficiency and quality of clinical research services.
- Attend conferences, seminars, and training sessions to stay updated on industry developments and best practices.
- Adhere to company and industry ethical standards and maintain confidentiality of sponsor and patient information.
- Represent IQVIA in a professional and positive manner at all times.
Bachelor's Degree In A Scientific Or Healthcare-Related Field: A Strong Educational Background In A Relevant Field Is Essential For An Experienced Clinical Research Associate (Cra) At Iqvia. A Bachelor's Degree In A Scientific Or Healthcare-Related Field Such As Biology, Nursing, Or Pharmacy Provides A Solid Foundation For Understanding The Complexities Of Clinical Research.
Minimum Of 3 Years Of Experience As A Cra: Iqvia Requires A Minimum Of 3 Years Of Experience As A Cra For Their Sponsor Dedicated Position. This Experience Demonstrates A Thorough Understanding Of The Clinical Research Process, Including Protocol Development, Site Management, And Data Collection And Analysis.
Excellent Communication And Interpersonal Skills: As A Cra, You Will Be Working With A Team Of Professionals From Various Backgrounds, As Well As Interacting With Study Site Staff And Study Participants. Strong Communication And Interpersonal Skills Are Crucial For Effective Collaboration And Building Relationships With Stakeholders.
Knowledge Of Regulatory Requirements And Guidelines: An Experienced Cra Should Have A Thorough Understanding Of Good Clinical Practice (Gcp) Guidelines And Other Relevant Regulatory Requirements. This Knowledge Is Essential For Ensuring That Clinical Trials Are Conducted In Compliance With Ethical And Legal Standards.
Attention To Detail And Strong Organizational Skills: The Role Of A Cra Involves Managing A Large Amount Of Data And Ensuring Its Accuracy And Completeness. Strong Attention To Detail And Organizational Skills Are Necessary To Effectively Oversee Multiple Study Sites And Ensure That All Documents And Data Are Properly Collected, Managed, And Reported.
Risk Management
Quality Control
Data collection
Regulatory compliance
Clinical monitoring
Site management
Electronic
Patient Recruitment
Protocol Review
Study Coordination
Protocol Adherence
Investigator Training
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Organization
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Experienced Clinical Research Associate, Sponsor Dedicated is $80,000 to $120,000 per year. Factors such as location, company size, and years of experience can affect the exact salary within this range.
Apply with Video Cover Letter Add a warm greeting to your application and stand out!
IQVIA, formerly Quintiles and IMS Health, Inc., is an American multinational company serving the combined industries of health information technology and clinical research.
Get interviewed today!
JobzMall is the world‘ s largest video talent marketplace.It‘s ultrafast, fun, and human.
Get Started