REGULATORY ASSOCIATE at K2 Staffing LLC

, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

13 May, 26

Salary

0.0

Posted On

12 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Documents, Clinical Trials, Attention to Detail, Interpersonal Skills, Planning, Organizational Skills, Communication Skills, Problem Solving, MS Office, Customer Service

Industry

Staffing and Recruiting

Description

K2 Medical Research is seeking a Regulatory Associate to support our facilities out of The Villages, FL. The Regulatory Associate is responsible for the development and maintenance of regulatory documents pertaining to the clinical trials conducted at K2 Medical Research. The position will manage all aspects of study start-up, modification submissions, ongoing reporting, and study close-out to the Institutional Review Board (IRB) and the clinical trial sponsor. This role requires collaborating and interfacing with a variety of teams and excellent attention to detail. Primary Responsibilities: * Prepare regulatory documents for new study submissions to IRB and sponsor * Maintain regulatory files at audit-ready status at all times by ensuring filing are up-to-date upon completion of the processing of new or revised documents * Report protocol deviations and serious adverse events to the IRB according to protocol and IRB requirements. * Receive, track, and distribute IND Safety Reports to the Principal Investigator for acknowledgement of review and file. Submit IND Safety Reports to the study-assigned IRB if submission is not handled by the sponsor * Inform clinical operations of new study approvals including at initiation, amendments, and consent forms upon receipt. Ensure documents are distributed to the clinical team as appropriate and filed * Communicate and update Sponsor with any revised site information and notify the IRB as required * Liaison with IRBs on a frequent basis to ensure resolution of outstanding submissions requests * Learn and utilize IRB electronic web portals for the processing of study submissions * Distribute IRB approvals on new study submission to the clinical team and sponsor for resolution of questions or Board requests * Manage the development of new Informed Consent Form drafts with the IRB, as needed, and ensure agreement with ICF language between K2 Medical Research Clinical Operations teams, IRB, and Sponsor * Obtain Clinical assignments from the Operations teams for the development of new Delegation of Authority Logs and inform teams of missing information or needs for updates to the Logs * Ensure protocol training is captured and returned to the regulatory department prior to the assigned staff members completing the Delegation of Authority Logs Ensure all regulatory binder or electronic regulatory platforms are updated at final monitoring closeout visits * Notification to Finance team as necessary to facilitate invoices * Inform assigned individuals of the need for archiving assistance of closed regulatory books at the defined time frame for long-term storage * Liaison with sponsor monitors during routine and closeout monitoring visits to ensure resolution of outstanding regulatory document requirements are attended to within an appropriate time frame * Schedule monitoring visits, prep books, and assign monitoring space as requested * Provide team assistance on all projects as needed * Assist in the tracking of the status of new study submissions status * Perform ad-hoc projects and/or general office duties as necessary * Other duties as assigned Knowledge, Skills, and Abilities: * Learn and support the organization goals, missions, and values * Good interpersonal, planning/organizational, and communication skills (written and oral) * Ability to handle multiple tasks/projects simultaneously * Attention to detail * Handles confidential information appropriately * Takes initiative and participates as a team player * Strong customer service skills * Ability to think critically, problem solve and take initiative when appropriate * Knowledgeable with MS Office and Outlook Qualifications: * Prefer 2 or more years of clinical research or regulatory experience * Bachelor's Degree and CCRP preferred Benefits: At K2, we value our employees and their professional and personal needs, and support these through our benefit offerings: * Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term disability and Life Insurance, Short Term Disability, Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs. * 401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested * PTO of 16 days per year, 17 days after the first year of FT employment * 9 paid Holidays Join the K2 Family: Where Compassion and Connection Lead the Way! At K2 Med, 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 thrive on empathy, a patient-first approach, and absolutely zero big egos (unless it's an ego about being extra kind, then we'll allow it!). We believe a supportive, caring experience is paramount for our patients, and that starts with you. We celebrate what makes you uniquely you! Your race, color, religion, marital status, age, national origin, or even your favorite snack (though we're partial to good research snacks) don't define your talent or fit here. If you need a little extra support or accommodation due to a disability, no sweat! Just reach out to our friendly team at Talent@k2med.com, and we'll ensure you have everything you need to shine.

Responsibilities

The Regulatory Associate is responsible for the development and maintenance of regulatory documents for clinical trials, managing study start-up, modification submissions, ongoing reporting, and study close-out. This role involves collaboration with various teams and ensuring compliance with IRB and sponsor requirements.