Clinical Research Assistant - job 1 of 2

As a Clinical Research Assistant at Care Access, you will take on a variety of responsibilities aimed at supporting clinical trials. This includes understanding and following Standard Operating Procedures, participating in recruitment and pre-screening events, and assisting with the identification of potential participants through medical records and study charts. You will also help recruit new participants by conducting phone screenings, obtaining informed consent, and completing required visit procedures under the direction of the Clinical Research Coordinator. Ensuring adherence to FDA regulations and Good Clinical Practices is crucial, and you'll be involved in data entry and maintaining site logs, among other administrative tasks.

To be considered for the Clinical Research Assistant position at Care Access, candidates should ideally have a minimum of one year of recent experience working in roles such as Medical Assistant, EMT, LPN, or Phlebotomist. Proficiency in phlebotomy and familiarity with medical and research terminology are essential. Candidates should also show strong organizational skills, the ability to work independently, and excellent communication abilities. A high degree of professionalism when interacting with patients and other research personnel is needed to excel in this role.

Yes, the Clinical Research Assistant at Care Access will be required to travel within the region for recruitment efforts and other responsibilities. While this role is primarily on-site, regular regional commutes are part of the job. However, overnight travel is minimal, typically less than 10%, making this a manageable aspect of the position while still allowing you to engage with diverse participants.

Essential skills for a Clinical Research Assistant at Care Access include excellent organizational abilities, strong communication skills, and a keen attention to detail. Candidates should also possess critical thinking and problem-solving skills, alongside a friendly and outgoing personality. Familiarity with Microsoft Office Suite and the ability to work independently with minimal supervision are also important for efficiently executing the responsibilities associated with conducting clinical trials.

As a Clinical Research Assistant at Care Access, there are ample opportunities for career advancement within the organization. This entry-level role is designed to equip you with the skills and knowledge necessary to transition into a Clinical Research Coordinator position in the future. As you gain experience and demonstrate your capabilities, you might find pathways to explore specialized roles in clinical research, such as Clinical Research Associate or project management positions, supporting the overall mission of Care Access.

In my previous role, I followed established clinical protocols closely and ensured compliance by maintaining awareness of all Standard Operating Procedures. I regularly reviewed protocols, participated in training sessions, and utilized checklists to help track compliance-related tasks, ensuring every step adhered to FDA regulations and Good Clinical Practices.

I approach recruitment challenges by being proactive and resourceful. I focus on understanding the study criteria thoroughly, which helps me identify the right participants more effectively. Additionally, I maintain strong communication with other research team members and explore various outreach strategies, like social media, local healthcare facilities, and community events to maximize recruitment efforts.

The most important quality for a Clinical Research Assistant is attention to detail. Being meticulous ensures that data collected is accurate and all compliance measures are followed. This quality significantly impacts the integrity of the research and can influence the outcomes, making it essential to deliver credible results.

I manage multiple tasks by prioritizing them based on deadlines and urgency. Utilizing organizational tools like to-do lists and calendar reminders helps me keep track of my responsibilities. I also believe in staying flexible, adapting to changes as they arise, and communicating effectively with my team to ensure all key tasks are completed on time.

In a previous role, I was part of a clinical trial team composed of individuals from various backgrounds. I facilitated open communication by encouraging everyone to share their ideas and perspectives. This diversity enriched our discussions and led to innovative solutions. We addressed any potential misunderstandings quickly and respectfully, reinforcing a strong collaborative environment.

Building rapport with study participants begins with showing genuine interest and empathy. I approach each interaction with a friendly demeanor, making sure to listen actively to their concerns and questions. Establishing trust is crucial, so I respect their time and provide clear explanations about the study, ensuring they feel comfortable and valued throughout the process.

To ensure high-quality data entry, I adopt a systematic approach. Verification is key; I double-check entries for accuracy before finalization. I also keep organized notes that correspond with collected data to prevent any discrepancies. Staying meticulous is vital to maintain the integrity of the trial data and ensure compliance with regulatory expectations.

Good Clinical Practices (GCP) are a set of internationally recognized ethical and scientific quality standards that guide clinical trials involving human subjects. Understanding GCP ensures that trials are conducted with the utmost care concerning participant rights, safety, and well-being. It encompasses proper methods for informed consent, data integrity, and the systematic management of trial protocols to uphold quality and credibility.

My motivation to work in clinical research stems from a passion for improving patient care. I find fulfillment in supporting studies that lead to groundbreaking treatments and understanding how they impact lives. Knowing that my contributions help bring innovative therapies to those in need drives my enthusiasm and commitment to the field.

To stay updated on industry advancements, I regularly read journals and attend webinars related to clinical research and GCP regulations. Networking with other professionals and engaging in training opportunities also helps me remain informed. Embracing continuous learning is essential in this constantly evolving field, and I appreciate sharing insights with my team to foster a collaborative learning environment.