About Company
Career.zycto is a dynamic organization committed to fostering the next generation of clinical research professionals. We believe in empowering new talent, providing a supportive environment where burgeoning Clinical Research Associates can thrive. Joining us means stepping into a world of impactful scientific discovery, guided by experienced mentors and cutting-edge methodologies. We’re dedicated to high-quality research, ethical practices, and the professional growth of every team member. If you’re passionate about making a real difference in healthcare through research, Career.zycto offers an unparalleled launchpad for your career.
Job Description
Are you eager to launch a rewarding career at the forefront of medical innovation? Career.zycto is seeking a highly motivated and detail-oriented Entry Level Clinical Research Associate to join our growing team in East Biloxi. This is an exceptional opportunity for individuals passionate about science and healthcare to contribute directly to advancing new therapies and improving patient lives.
As an Entry Level Clinical Research Associate, you will play a crucial supporting role in the planning, execution, and oversight of clinical trials. Under the guidance of experienced Senior CRAs and Project Managers, you will learn the critical aspects of clinical trial monitoring, regulatory compliance, and data integrity. This role is designed to provide comprehensive training and mentorship, equipping you with the foundational knowledge and practical skills necessary to excel in the clinical research industry.
Your journey will involve understanding complex study protocols, ensuring adherence to Good Clinical Practice (GCP) guidelines, and meticulous documentation practices. You will gain hands-on experience in supporting site initiation, routine monitoring visits, and close-out activities. This role is perfect for someone who is a quick learner, possesses excellent organizational skills, and has a keen eye for detail. You will collaborate closely with study sites, investigators, and internal teams, acting as a vital link in the communication chain to ensure smooth trial operations and the collection of high-quality data.
We offer a structured training program that will introduce you to all facets of clinical trial management, from protocol understanding to regulatory submissions. This is not just a job; it’s an investment in your future, providing a clear pathway for professional development and advancement within the clinical research landscape. If you’re ready to make a tangible impact and grow with a company that values integrity, collaboration, and scientific excellence, we encourage you to apply.
Key Responsibilities
- Assist in the preparation and review of study-related documentation, including study plans, case report forms, and informed consent forms.
- Support the conduct of site qualification, initiation, interim monitoring, and close-out visits under direct supervision.
- Verify adherence to study protocols, Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements.
- Review source documents and Case Report Forms (CRFs) for accuracy, completeness, and consistency.
- Assist in resolving data queries and ensuring data integrity.
- Maintain up-to-date knowledge of clinical trial processes, relevant regulations, and therapeutic areas.
- Communicate effectively with study site personnel and internal project teams.
- Participate in team meetings and training sessions to enhance clinical research knowledge and skills.
- Support the preparation and maintenance of the Trial Master File (TMF) and Investigator Site File (ISF).
Required Skills
- Bachelor's degree in a life science, health-related field, or nursing.
- Strong interest in clinical research and drug development.
- Excellent written and verbal communication skills.
- Exceptional attention to detail and organizational abilities.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work both independently and as part of a collaborative team.
- Strong problem-solving skills and a proactive attitude.
- Willingness to travel as required (typically 25-50% once fully trained).
Preferred Qualifications
- Prior internship or volunteer experience in a research, healthcare, or laboratory setting.
- Knowledge of medical terminology.
- Certification in Good Clinical Practice (GCP).
- Familiarity with regulatory guidelines (e.g., FDA, ICH).
Perks & Benefits
- Comprehensive health, dental, and vision insurance.
- Generous paid time off and holidays.
- 401(k) retirement plan with company match.
- Structured training and mentorship programs.
- Opportunities for continuous professional development and career advancement.
- Employee assistance program.
- Life and disability insurance.
- Collaborative and supportive work environment.
How to Apply
To apply for this exciting Entry Level Clinical Research Associate position and embark on a fulfilling career with Career.zycto, please click on the application link below. We look forward to reviewing your qualifications and learning more about your passion for clinical research.
