Job Description

Job Description

Job Description

Description:

The SerenaGroup is growing fast, and we’re looking for a Clinical Research Associate who thrives in a dynamic environment. If you’re a natural organizer, love collaborating with smart people, and have a knack for quality, safety, compliance, and ethics, you might be the person we’re looking for.

As a Clinical Research Associate, you’ll play a key role in organizing and monitoring clinical trials from start to finish. Your work ensures studies are conducted safely, ethically, and complying with all relevant protocols.

Key Responsibilities

• Supervising study sites and activities to ensure everything is running according to industry standards and the specific terms of each study.
• Collecting and validating data collection forms, also known as case report forms, is essential to maintaining the accuracy and integrity of clinical data.
• Screening potential study participants by reviewing medical records, conducting interviews, and following up with healthcare providers.
• Coordinating with ethics committees to protect all research subjects’ rights, safety, and well-being and ensure compliance with ethical guidelines.
• Keeping detailed records of all research activities, including regulatory forms, drug dispensation records, case reports, and consent forms.
• Preparing final study reports, occasional manuscripts or publications, and New Drug Applications (NDAs) and Biological License Applications (BLAs).
• Make sure clinical case data is correctly transmitted to data management centers, review any questions or issues, and clarify or update data as needed.
• Overseeing, training, and supporting research, technical, and administrative staff—including hiring, goal setting, and managing workloads.

Success in this role means being organized, detail-oriented, and proactive in keeping studies running smoothly and ethically. If you’re ready to make an impact in clinical research, we’d love to hear from you.

What Makes You a Great Fit

• You pick up new skills fast and love learning on the job.
• Details matter to you—you like to monitor work for quality while ensuring safety and compliance.
• You’re adaptable and thrive when things change (because they will).
• Ethical behavior is at the top of your mind.
• You take initiative and find ways to improve processes rather than just waiting for instructions.
• You’re motivated by meaningful work and share our values.
• You solve problems with logic and creativity.
• You’re a team player who builds trust and drives a positive, collaborative vibe.
• You have technical know-how from education, training, or hands-on experience.
• You pride yourself on a strong work ethic and high standards.

Why Join SerenaGroup?

We’re not just growing—we’re building something special. As we expand, you’ll have the chance to take on new challenges, develop your skills, and make a real impact. We value curiosity, initiative, and people who care about doing great work.

Ready to help shape the future of clinical research? Apply now and let’s talk.

Qualifications

• Associate degree or equivalent relevant experience.
• Confident with basic math—decimals, fractions, the whole deal.
• Clear and effective communicator, both written and spoken.
• Intermediate reasoning and problem-solving ability.

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