Clinical Research Associate (Monitor) at SerenaGroup Inc

Atlanta, Georgia, United States -

Full Time

Start Date

Immediate

Expiry Date

28 Jan, 26

Salary

80000.0

Posted On

30 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Wound Care Nursing, Data Collection, Communication, Problem Solving, Organizational Skills, Ethical Behavior, Teamwork, Attention to Detail, Regulatory Compliance, Clinical Trials, Training, Record Keeping, Data Management, Flexibility, Proactivity, Quality Assurance

Industry

Medical and Diagnostic Laboratories

Description

Description DO YOU HAVE WOUND CARE NURSING EXPERIENCE AND ARE SEEKING A NEW ROLE? Explore the Clinical Research Associate (Monitor) position with SernaGroup, Inc Salary Range - $70,000 to $80,000 annually The SerenaGroup is growing rapidly, and we are searching for a Clinical Research Associate who excels in a fast-paced environment. If you are a natural organizer, enjoy working with bright people, and have a talent for quality, safety, compliance, and ethics, you could be the person we need. As a Clinical Research Associate, you will play a vital role in organizing and overseeing clinical trials from beginning to end. Your work guarantees that studies are conducted safely, ethically, and in accordance with all relevant protocols. ESSENTIAL FUNCTIONS Supervising study sites and activities to ensure everything functions according to industry standards and the specific terms of each study. Collecting and validating data collection forms, also known as case report forms, to ensure the accuracy and integrity of clinical data. Screening potential study participants through reviewing medical records, conducting interviews, and following up with healthcare providers. Coordinating with ethics committees to safeguard all research subjects' rights, safety, and well-being and ensure adherence to ethical guidelines. Keeping detailed records of all research activities, including regulatory forms, drug dispensation logs, case reports, and consent forms. Preparing final study reports, occasional manuscripts or publications, and New Drug Applications (NDAs) and Biological License Applications (BLAs). Ensuring that clinical case data is properly transmitted to data management centers, reviewing any questions or issues that arise, and clarifying or updating data as necessary. Overseeing, training, and supporting research, technical, and administrative staff—including hiring, goal setting, and workload management. Success in this role involves being organized, detail-oriented, and proactive to ensure studies run smoothly and ethically. If you’re ready to make an impact in clinical research, we look forward to hearing from you. What Makes You a Strong Candidate? You quickly pick up new skills and enjoy learning while working. Details matter to you—you prefer to oversee work to maintain quality while guaranteeing safety and compliance. You’re flexible and succeed when things shift (since they will). Ethical behavior is your top priority. You proactively identify opportunities to enhance processes instead of waiting for instructions. You’re motivated by meaningful work and share our values. You approach problems with logic and creativity. You’re a team player who fosters trust and promotes a positive, collaborative environment. You have technology. clinical know-how, whether gained through education, training, or hands-on experience. You take pride in having a strong work ethic and maintaining high standards. Requirements QUALIFICATIONS 1-2 years of wound care nursing experience. Associate degree or equivalent experience relevant to the role. Confident in basic math—decimals, fractions, and everything. Clear and effective communicator in both writing and speaking. Intermediate reasoning and problem-solving skills. Why Join SerenaGroup? We’re not just growing—we’re building something special. As we expand, you’ll have the opportunity to take on new challenges, develop your skills, and make a meaningful impact .We value curiosity, initiative, and people who care about doing great work. Ready to help shape the future of clinical research? Apply today and let’s discuss.

Responsibilities

As a Clinical Research Associate, you will oversee clinical trials to ensure they are conducted safely and ethically. You will supervise study sites, validate data, and coordinate with ethics committees while maintaining detailed records of research activities.