Clinical Research Associate – Imaging Studies – Los Angeles, CA
Are you a detail-oriented and skilled professional with a passion for medical research and imaging studies? We are looking for a Clinical Research Associate (CRA) to join our team in Los Angeles, CA. This is a unique opportunity to be part of cutting-edge clinical trials in the field of imaging, contributing to the advancement of medical science and patient care. If you have experience in clinical research, imaging studies, and data management, this role is perfect for you.
Join a Leading Medical Research Team in Los Angeles
We are a pioneering medical research organization seeking a Clinical Research Associate to support our imaging studies team in Los Angeles, CA. The ideal candidate will have a strong background in clinical research, with a focus on imaging technologies and data analysis. As a CRA, you will play a crucial role in the design, execution, and monitoring of clinical trials, ensuring the integrity and accuracy of data while adhering to regulatory guidelines. If you’re ready to contribute to groundbreaking research and work in a dynamic environment, this is an exciting opportunity to further your career.
Key Responsibilities of the Clinical Research Associate (CRA) – Imaging Studies
Study Coordination & Monitoring: Manage and oversee clinical trials focused on imaging technologies, ensuring compliance with study protocols, regulatory guidelines, and ethical standards. Monitor trial progress, recruitment, and patient safety while ensuring high-quality data collection.
Data Management & Analysis: Assist in the collection, management, and analysis of clinical trial data, ensuring the accuracy and integrity of imaging data. Coordinate with cross-functional teams to ensure timely data entry, proper documentation, and compliance with Good Clinical Practice (GCP) guidelines.
Regulatory Compliance: Ensure that clinical trials comply with all applicable regulations, including FDA, ICH, and GCP standards. Prepare and maintain regulatory documents, including informed consent forms, ethics committee approvals, and trial master files.
Site & Investigator Relations: Establish and maintain positive relationships with clinical trial sites and investigators. Provide guidance and support to clinical site staff to ensure efficient trial execution and resolve any site-specific issues that arise during the trial process.
Quality Assurance: Conduct site visits and monitoring visits to ensure that clinical trials are conducted in accordance with approved protocols and regulatory requirements. Identify and address any potential issues related to data quality, patient safety, or site performance.
Patient Safety & Ethical Standards: Ensure that patient safety is prioritized throughout the clinical trial process. Monitor adverse events and report them to relevant parties, maintaining compliance with safety protocols and ethical standards.
Study Documentation & Reporting: Maintain accurate and comprehensive study documentation, including trial protocols, case report forms (CRFs), monitoring reports, and study correspondence. Prepare detailed reports and contribute to the preparation of final study reports and regulatory submissions.
Collaboration & Communication: Work closely with internal teams, including medical, regulatory, and clinical operations, to ensure smooth execution of imaging studies. Communicate effectively with stakeholders, including investigators, site coordinators, and regulatory authorities, to ensure alignment and progress.
Continuous Improvement: Identify areas for improvement within clinical trial operations and contribute to process optimization. Stay updated on industry trends, regulatory changes, and new technologies related to imaging and clinical research to ensure the company remains at the forefront of innovation.
What the Client is Looking for in You
As the Clinical Research Associate (CRA) – Imaging Studies, the client is seeking a dedicated and detail-oriented professional with a strong background in clinical research, particularly in imaging studies. You should be a proactive team player who excels in managing complex studies, ensuring data accuracy, and maintaining regulatory compliance. The ideal candidate will demonstrate a passion for advancing medical research and a commitment to contributing to innovative imaging solutions in clinical trials.
Experience in Clinical Research and Imaging Studies
The client is looking for a candidate with a solid foundation in clinical research, specifically in the field of imaging technologies. A background in conducting, managing, and monitoring clinical trials is essential, as is an understanding of imaging modalities used in medical studies. Experience working with clinical trial protocols, case report forms (CRFs), and regulatory submissions is highly valued.
Strong Knowledge of Regulatory Guidelines
The ideal CRA candidate must possess a deep understanding of regulatory frameworks, including Good Clinical Practice (GCP), FDA regulations, and ICH guidelines. The client values professionals who can navigate the complexities of clinical trials while ensuring compliance with both internal and external standards. Familiarity with ethical standards and patient safety protocols is essential.
Attention to Detail and Data Integrity
In clinical research, accuracy is paramount. The client seeks a CRA who can meticulously manage data, ensuring its integrity and consistency throughout the trial process. You should have a keen eye for detail and be capable of identifying discrepancies or issues early, ensuring high-quality results. The ability to analyze and report on clinical data is crucial for this role.
Excellent Communication and Interpersonal Skills
The role requires strong communication and collaboration skills, as you will interact with various stakeholders, including clinical site staff, investigators, and cross-functional teams. The client is looking for a CRA who can clearly present findings, provide guidance, and maintain professional relationships with all parties involved in the study.
Problem-Solving and Critical Thinking Abilities
The ideal candidate should possess the ability to proactively address challenges and resolve issues that may arise during clinical trials. Whether it’s troubleshooting logistical issues, overcoming recruitment hurdles, or managing unforeseen study deviations, you should have the problem-solving skills to keep studies on track.
Commitment to Patient Safety and Ethical Research Practices
Patient safety is always the priority in clinical trials. The client values candidates who uphold ethical standards and ensure the protection of trial participants. You should be vigilant about monitoring adverse events, reporting them promptly, and ensuring compliance with all relevant safety protocols.
Ability to Work Independently and in a Team Environment
While the CRA will be expected to work independently in monitoring studies and managing data, collaboration is key to the success of clinical trials. The client seeks someone who can balance both working autonomously and contributing effectively to a larger team, ensuring the smooth execution of clinical research projects.
Adaptability and Willingness to Learn
The medical research field is continually evolving, and the client is looking for someone who is adaptable and eager to stay current with emerging trends in clinical research, imaging technologies, and regulatory changes. The ability to quickly learn new systems and technologies will be a key asset in this role.
FAQs About the Role – Clinical Research Associate (CRA) – Imaging Studies
What are the key responsibilities of the Clinical Research Associate (CRA) in this role?
As a Clinical Research Associate (CRA) in Imaging Studies, you will be responsible for managing and monitoring clinical trials that involve imaging technologies. This includes coordinating study activities, ensuring regulatory compliance, managing data collection, and maintaining accurate study documentation. You will work closely with clinical trial sites, investigators, and cross-functional teams to ensure the successful execution of imaging studies. Your role will also involve ensuring patient safety, monitoring adverse events, and preparing study reports.
What qualifications and experience are required for this position?
The ideal candidate should have a background in clinical research, preferably with experience in imaging studies. A strong understanding of regulatory guidelines, such as GCP, ICH, and FDA regulations, is essential. Experience in managing clinical trials, data analysis, and site monitoring is highly preferred. A degree in life sciences, medical research, or a related field is required, and additional certifications in clinical research (e.g., ACRP, SOCRA) are a plus.
What technical skills are essential for this role?
The CRA should have proficiency in clinical trial management software, data analysis tools, and regulatory documentation systems. A solid understanding of imaging modalities and the ability to interpret imaging data is crucial. Familiarity with electronic data capture (EDC) systems and knowledge of clinical trial protocols and case report forms (CRFs) is also required.
What challenges can I expect in this role?
In this role, you will face challenges such as managing the complexities of imaging data, ensuring data accuracy, and handling the logistical aspects of clinical trial coordination. You will need to navigate regulatory requirements and address any discrepancies or issues that arise during the trial process. Additionally, maintaining patient safety and managing potential adverse events in clinical trials can be a significant challenge.
What impact will the CRA have on the clinical trials and research outcomes?
The CRA will play a vital role in ensuring the accuracy and integrity of data collected during imaging studies, which directly impacts the success of the clinical trials. By ensuring compliance with protocols and regulatory standards, you will help maintain the credibility of the study results, which are crucial for advancing medical research and patient care. Your attention to detail and ability to solve problems efficiently will be essential for the successful completion of clinical studies.
What is the company’s culture and work environment like?
The company offers a collaborative and research-driven environment where innovation and precision are highly valued. You will be working in a fast-paced setting, interacting with medical professionals, researchers, and clinical teams. The company encourages continuous learning, professional development, and a team-oriented approach to achieving clinical research goals. They value integrity, transparency, and a commitment to patient safety in all aspects of their research.
What Remuneration Can You Expect from This Job?
As a Clinical Research Associate (CRA) – Imaging Studies in Los Angeles, CA, you can expect a competitive and comprehensive compensation package. The remuneration for this role is designed to reflect your experience, expertise, and the importance of your contributions to the success of the clinical trials and research studies. The compensation typically includes the following components:
- Base Salary
The base salary for a Clinical Research Associate (CRA) specializing in imaging studies typically ranges between $60,000 to $100,000 annually, depending on your experience, education, and the scope of your responsibilities. Professionals with advanced experience and certifications in clinical research or imaging may expect higher salaries within this range.
- Performance-Based Bonuses
Many companies offer annual performance-based bonuses to their clinical research staff, tied to individual and team performance metrics, as well as the successful execution of clinical trials. These bonuses can vary, but typically range from 5% to 15% of the base salary, depending on project success, recruitment targets, and data integrity.
- Health & Wellness Benefits
In addition to the base salary, CRA roles often come with comprehensive health and wellness benefits, including:
- Medical, dental, and vision insurance
- Mental health support programs
- Paid time off (PTO) and sick leave
These benefits ensure your well-being while you focus on driving research success.
- Retirement Plans & Savings
Most organizations provide retirement benefits, such as a 401(k) plan, with employer contributions or matching options. This allows you to plan for your future while contributing to groundbreaking medical research.
- Professional Development & Continuing Education
As part of your remuneration package, you may receive support for professional development, including reimbursement for certifications (such as ACRP or SOCRA) and continuing education programs. This ensures you remain at the forefront of clinical research and imaging technologies, which can enhance your career growth and advancement.
- Relocation Assistance & Signing Bonuses
For candidates relocating to Los Angeles, companies may offer relocation assistance to cover moving expenses. Additionally, some companies may provide signing bonuses for highly qualified candidates, especially if they bring specialized skills or experience in imaging studies. Signing bonuses can range from $5,000 to $15,000, depending on the role and candidate profile.
Total Compensation Potential
When combining base salary, performance-based bonuses, benefits, and professional development opportunities, the total compensation package for a CRA in Imaging Studies can range from $70,000 to $120,000 annually. For candidates with extensive experience and specialized skills, total compensation could exceed this range, especially if the position offers additional perks or performance incentives.
How to Apply
If you are a dedicated and experienced Clinical Research Associate with a focus on imaging studies, we invite you to apply for the Clinical Research Associate – Imaging Studies role in Los Angeles, CA. This is an exciting opportunity to contribute to cutting-edge clinical trials and play a vital role in advancing medical research and patient care.
To apply, please submit your resume along with a cover letter that outlines your experience in clinical research, particularly in imaging studies, data management, and regulatory compliance. Highlight your expertise in coordinating clinical trials, monitoring patient safety, and ensuring data integrity. Additionally, share any relevant certifications or training that demonstrate your commitment to staying at the forefront of the clinical research field.
This role offers a rewarding career in the medical research field, where you will make a direct impact on the success of clinical trials and the development of innovative imaging technologies. Apply today to take the next step in your clinical research career as a Clinical Research Associate – Imaging Studies in Los Angeles, CA!
For more information or to explore similar opportunities, visit our Clinical Research Careers Page.
Tags: Clinical Research Associate | Clinical Trials | Imaging Studies | Medical Research | Regulatory Compliance | Patient Safety | Data Management | Clinical Research Jobs | Imaging Technologies | Clinical Research Careers
