Regulatory Associate

Automatic Data Processing, Inc.; Florida; On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Four-day work week

Health insurance

Dental + vision

401(k) with employer match

Paid time off & holidays

Job summary

K2 Medical Research in Maitland, FL, seeks a Regulatory Associate for full-time, non-patient-facing regulatory operations across multiple trials. You will manage IRB submissions, DOA logs, and study start-up timelines, ensuring GCP and FDA compliance.

This role emphasizes organized workflow, cross-team collaboration, and meticulous record-keeping to support trial activations. Join a patient-first organization that values process excellence and offers a four-day work week, comprehensive benefits,

Qualifications

• Site-level regulatory experience in clinical trials is required.
• Strong understanding of IRB submissions, regulatory workflows, and DOA logs.
• Organized, detail-oriented, with excellent multi-tasking and timeline management.

Responsibilities

• IRB Oversight & Submissions: Prepare, submit, and track initial study submissions, protocol amendments, continuing reviews, safety reports, and ICFs to IRBs.
• DOA Logs: Maintain and audit DOA logs, ensuring training records and regulatory binder documents are accurate and compliant.
• Study Start-Up & Timeline Management: Drive start-up workflows from packet receipt through SIV and activation; manage trial trackers.
• Regulatory Compliance & Audits: Maintain electronic regulatory documents in compliance with GCP, FDA regs; serve as regulatory contact.
• High-Volume Multitasking & Tracking: Manage multiple trials across study lifecycles; follow-up to close items efficiently.

Skills

eReg systems

Study tracking

Regulatory coordination

Attention to detail

Tools

eTMF

Excel

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Regulatory Associate

Full Time Professional Maitland, FL, US

At K2 Medical Research , we are transforming healthcare by delivering tomorrow’s treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. Our culture is grounded in clinical excellence and a patient-first mission. We are seeking mission-driven individuals ready to play a meaningful role in bringing life-changing treatments to the patients who need them most.

K2 is seeking an organized, detail-oriented Regulatory Associate to manage site-level regulatory operations, protocol activations, and study start-up compliance out of our clinic in Maitland, FL.

This is a non-patient-facing, highly process-driven role ideal for structured, methodical professionals who thrive in task organization, tracker management, and compliance oversight.

Primary Responsibilities:

• IRB Oversight & Submissions: Prepare, submit, and track initial study submissions, protocol amendments, continuing reviews, safety reports, and informed consent forms (ICFs) to central and local Institutional Review Boards (IRBs).
• Delegation of Authority (DOA) Logs: Maintain and audit Delegation of Authority (DOA) logs, ensuring all site staff signatures, training records, and regulatory binder documents are accurate and fully compliant prior to study participation.
• Study Start-Up & Timeline Management: Drive study start-up workflows from initial packet receipt through site initiation visits (SIV) and study activation. Proactively manage trial trackers and study timelines to prevent bottlenecks.
• Regulatory Compliance & Audits: Maintain essential electronic regulatory documents (eReg) in compliance with Good Clinical Practice (GCP), FDA regulations, and Sponsor guidelines. Serve as the primary regulatory point of contact for Sponsor/CRO monitors and auditors.
• High-Volume Multitasking & Tracking: Manage high-volume, concurrent clinical trials across varying stages of study lifecycle. Drive rigorous follow-up with internal teams, Sponsors, and IRBs to ensure actionable items are closed efficiently.

Knowledge, Skills, and Abilities:

• Strong technical proficiency in eReg systems, clinical trial software, and advanced study-tracking tools (Excel/eTMF).
• In-depth, operational understanding of IRB submission processes, regulatory workflows, and DOA log maintenance.
• Exceptional organization, multi-tasking, and timeline-management capabilities in a high-volume environment.
• Strong follow-up skills with high accountability and attention to detail.
• Support the organization's goals, missions, and values .
• Ability to work collaboratively across departments to ensure seamless operational flow .

Qualifications:

• Site-Level Regulatory Experience: Must have site-level regulatory exposure in clinical trials. Experience in Study Start-Up processes is strongly preferred.
• Diverse Backgrounds Encouraged:Candidates with strong Clinical Research Coordinator (CRC) or Project Manager (PM) backgrounds who possess significant regulatory exposure are encouraged to apply.
• Sponsor / CRO / CRA Backgrounds:Transferable candidates from Sponsor, CRO, or CRA roles seeking site-level operational roles are welcome to apply (salary alignable with site-level structures).

Your growth and well-being are our priority. Our comprehensive benefits package for full-time employees includes medical, dental, and vision options, supplemental insurance plans, 401(k) with immediate employer match, generous paid time off, and paid holidays. Most notably, we support a healthy work-life balance through a four-day work week, consisting of 10-hour shifts from Monday through Thursday. Fridays are reserved only for critical business needs or administrative tasks; otherwise, they are your chance to kick-start your weekend.

Join the K2 Family: Where Compassion and Connection Lead the Way! At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff.

We are an equal opportunity employer. We celebrate what makes you uniquely you and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital, or veteran statuses.

We value the differences among our team members and are committed to providing reasonable accommodations for qualified individuals with disabilities. If you require a reasonable accommodation to participate in the job application or interview process, please contact [e-mail]. We are here to ensure you have the support and tools you need to shine.