About Company
Career.supersecrets is at the forefront of driving innovation in clinical research, championing meticulously collected data and fostering passionate team collaboration. For a Junior Clinical Research Coordinator, this translates into a truly supportive environment where foundational skills are not only valued but actively honed for accelerated professional growth. We pride ourselves on offering unparalleled mentorship, broad exposure to diverse clinical trials, and a vibrant culture that consistently celebrates curiosity and groundbreaking contributions. Join us to directly contribute to life-changing medical advancements, making a tangible difference in patient lives from your very first day.
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Job Description
Are you passionate about making a tangible difference in healthcare and eager to kickstart your career in clinical research? Career.supersecrets is seeking a motivated and detail-oriented Junior Level Clinical Research Coordinator to join our dynamic, remote team. This is an exceptional opportunity for an individual with foundational knowledge in clinical research to gain hands-on experience, working alongside seasoned professionals to advance medical science. As a Junior CRC, you will play a critical role in supporting the planning, coordination, and execution of clinical trials, ensuring compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. While this is a remote position, we are specifically looking for candidates residing in Mesa, Arizona, to foster a strong regional team connection through occasional local meetings or training sessions, as necessary. This role offers comprehensive training and mentorship, guiding you through the complexities of patient recruitment, data management, regulatory documentation, and ethical conduct of studies. You will be instrumental in maintaining organized study files, preparing for monitoring visits, and contributing to the overall success of our research initiatives. We value proactive learning, strong communication skills, and a commitment to precision. If you’re ready to grow your expertise in a supportive, innovative, and impactful environment, this remote role is designed for your success. Embark on a rewarding career path where your contributions directly influence the development of new treatments and therapies, ultimately improving global health outcomes.
Key Responsibilities
- Assist in the preparation and submission of regulatory documents to Institutional Review Boards (IRBs) and other relevant bodies.
- Support patient recruitment efforts, including screening potential participants for eligibility against study protocols.
- Schedule and coordinate patient visits, ensuring all necessary procedures and assessments are completed accurately.
- Maintain accurate, comprehensive, and up-to-date study participant records, case report forms (CRFs), and source documents.
- Collect, record, and track research data, ensuring data integrity and adherence to protocol requirements.
- Assist in preparing for and participating in monitoring visits, audits, and inspections by sponsors and regulatory authorities.
- Ensure all research activities comply with Good Clinical Practice (GCP) guidelines, HIPAA regulations, and study protocols.
- Communicate effectively with study participants, investigators, and other research staff.
- Assist with the management and accountability of study-related materials and equipment.
- Participate in ongoing training and educational opportunities to stay current with clinical research best practices and regulations.
Required Skills
- Bachelor’s degree in a life science, healthcare-related field, or equivalent experience.
- Basic understanding of clinical research principles, methodologies, and terminology.
- Familiarity with medical terminology and standard office software (Microsoft Office Suite).
- Exceptional organizational skills and meticulous attention to detail.
- Strong verbal and written communication abilities.
- Ability to work independently in a remote setting while remaining a collaborative team player.
- Proven ability to manage multiple tasks and prioritize effectively.
- Resident of Mesa, Arizona.
Preferred Qualifications
- Prior experience (e.g., internship, volunteer work) in a clinical or research setting.
- Knowledge of ICH-GCP guidelines and regulatory requirements (e.g., FDA).
- Certification in clinical research (e.g., CCRP, CCRC, ACRP-CP) is a plus, but not required for this junior role.
- Experience with Electronic Data Capture (EDC) systems.
- Bilingual proficiency (especially Spanish) is an asset.
Perks & Benefits
- Competitive salary and performance bonuses.
- Comprehensive health, dental, and vision insurance.
- Generous paid time off and holidays.
- 401(k) retirement plan with company match.
- Dedicated budget for professional development and continuing education.
- Flexible remote work environment.
- Supportive mentorship program for career growth.
- Opportunity to work on groundbreaking research with a passionate team.
- Employee assistance program.
How to Apply
If you are ready to launch your career in clinical research and meet the qualifications for this remote position, we encourage you to apply. Please click on the application link below to submit your resume and a cover letter detailing your interest and relevant experience. Your cover letter should highlight why you are a great fit for a junior-level remote CRC role with Career.supersecrets. We look forward to reviewing your application!
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