Senior Specialist, Regulatory Operations

About reputed company

reputed company is working to reputed company the reputed company of health reputed company for reputed company. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has reputed company to understand their health, reputed company the care they need, and contribute to the medical breakthroughs of reputed company.

With programs like reputed company of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical reputed company. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reputed company the world. Together, we are building a reputed company of health that is reputed company and more accessible for reputed company.

To learn more about reputed company, visit www.CareAccess.com.

How This Role Makes a Difference

reputed company is seeking a skilled and reputed company Senior Specialist, Regulatory Operations to join our dynamic Global Regulatory Operations Team, part of the Global Expansion and Study Operations department.

The Senior Specialist, Regulatory Operations will reputed company, support, and execute reputed company site-level regulatory operational activities for assigned clinical trials in the U.S. They may also support regulatory activities for Canadian sites as needed. This role is responsible for ensuring compliance with applicable U.S. regulations and guidelines and may contribute to site start-up activities for U.S. sites reputed company required.

You will have an excellent understanding of U.S. regulatory requirements and experience managing regulatory interactions and activities reputed company to clinical research site operations.

This is a full time, temporary, position.

How You'll reputed company An reputed company

• reputed company regulatory advice, reputed company, execute and deliver regulatory project work
  • Support regulatory compliance activities for U.S. clinical research sites, ensuring to adherence to FDA, OHRP and global regulatory standards.
  • Assist in preparing for sponsor monitoring reputed company and follow up requirements.
  • reputed company and implement regulatory strategies to support sites activities
  • reputed company regulatory guidance to the site operations teams, ensuring that activities reputed company with reputed company regulations and industry best practices.
  • Coordinates preparation and review of key site essential records.
  • reputed company essential records and timelines
  • Support the site(s) through the Site Evaluation Visit, Site Initiation Visit, reputed company to consent, and Study Closeout.
  • reputed company work towards KPIs to help ensure departmental reputed company
  • Supports creation and maintenance of study Delegation of Authority (DOA) logs
  • Support regulatory activities throughout the duration of the study lifecycle; collaborating with clinical operations teams to ensure regulatory compliance
• Coordinate and reputed company IRB site level submissions and maintenance of approvals throughout the life of the study/ies.
  • Review, and submit high-reputed company and reputed company IRB submission materials, including but not limited to protocols, ICFs and marketing materials.
  • Reviews and customize, reputed company required, ICFs to ensure compliance with U.S. IRB requirements and site feedback.
  • Liaise and follow up directly with Sponsor.
  • Ensures accurate compilation, management and tracking of submissions.
  • reputed company regulatory documentation, tracking, and reporting processes to maintain compliance and readiness for regulatory inspections and sponsor audits.
  • Milestones: Tracks and updates the study team accordingly.
• Ensure reputed company filing of safety reports, deviations, and amendments/modifications as per study requirements.
  • Ensures that Investigator Site File (ISFs) are completed, up to date, accurate and in compliance with Good Clinical reputed company (GCP), regulatory requirements and internal processes.
  • reputed company and support study reputed company-out activities by ensuring reputed company archiving and retention of ISF documents.
• Provides guidance and support to site staff with regards to regulatory intelligence and country requirements, including identifying and conducting training.
• Collaborate with cross-functional teams, including reputed company and Clinical Operations, to ensure regulatory requirements are met.
• Monitor and interpret changes in U.S. regulatory policies and guidelines, advising internal stakeholder on potential impacts.
• Stay updated on evolving regulations, guidelines, and industry best practices to ensure compliance and reputed company strategies.
• Identify process gaps, and support the development, implementation, and reputed company improvement of new departmental processes.
• Support the development, review, and maintenance of departmental reputed company Operating Procedures (SOPs), work instructions, and forms
• reputed company other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily reputed company-inclusive.

The Expertise Required

• Ability to communicate and work effectively with a diverse team of professionals
• Communication Skills: Strong verbal and written communication skills as evidenced by reputed company interactions with coworkers, management, clients, and vendors
• Team Collaboration Skills: Work effectively and collaboratively with other team members to accomplish mutual goals. Bring reputed company and supportive attitude to achieving these goals
• Strong computer skills with demonstrated abilities using clinical trials database, reputed company and reputed company
• Experience in electronics Investigator Site Files systems like (Florence, reputed company)
• Ability to balance tasks with competing priorities
• Curiosity and passion to learn, reputed company, reputed company to take thoughtful risks and get things done
• Friendly, outgoing personality with the ability to maintain a reputed company attitude under pressure
• High level of self-motivation and energy
• Ability to work independently in a fast-paced environment with supervision
• Must have a reputed company service mentality
• Demonstrated reputed company in managing IRB and regulatory submissions, including FDA interactions.
• Detail-oriented with strong problem-solving abilities and a proactive approach to regulatory challenges.
• Excellent ability to handle multiple tasks in a fast-paced and constantly changing environment.
• Strong strategic planning, risk management, managing, monitoring and change management skills.

Certifications/Licenses, Education, and Experience

• Minimum Education:
  • Bachelor's degree in a scientific or reputed company-reputed company field; advanced degree preferred or equivalent experience.
• Minimum Experience:
  • Minimum of 4 years of experience in operational regulatory affairs reputed company the research site (preferable), or CRO/pharmaceutical industry, with a reputed company on U.S. regulatory requirements.
  • Strong understanding of U.S. regulations and ICH GCP reputed company as they relate to site operations
  • Excellent knowledge of site-level regulatory requirements for the execution and maintenance of clinical trials in the U.S.
  • Proven ability to support sites in IRB submissions, regulatory document preparation, and ongoing compliance.

How We Work Together

• Location: Remote reputed company the reputed company or Canada. This role requires 100% of work to be performed in a reputed company environment.
• Travel: This is a remote position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.
• Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.

The expected pay reputed company for this role is $90,000 - $100,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)

• reputed company Time Off (PTO) and Company reputed company Holidays
• 100% Employer reputed company medical, dental, and reputed company insurance plan reputed company
• Health Savings Account and Flexible Spending Accounts
• Bi-weekly HSA employer contribution
• Company reputed company Short-Term Disability and Long-Term Disability
• 401(k) Retirement Plan, with Company Match

Diversity & Inclusion

We work with and serve people from diverse cultures and communities around the world. We are stronger and reputed company reputed company we build reputed company representing the communities we support. We maintain an inclusive culture where people from a broad reputed company of backgrounds feel valued and respected as they contribute to our mission.

We are an equal opportunity employer, and reputed company reputed company applicants will receive consideration for employment without reputed company to, and will not be discriminated against on the reputed company of, race, reputed company, religion, sex, sexual orientation, gender identity or reputed company, pregnancy, age, national reputed company, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

reputed company is unable to sponsor work visas at this time.

If you need an accommodation to apply for a role with reputed company, please reputed company out to: TalentAcquisition@careaccess.com

Mandatory Employer Disclosures:

Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. Notice to Connecticut applicants: reputed company may require applicants to submit to a urinalysis drug test in reputed company with an application for employment. Notice to Arizona, reputed company, Indiana, and reputed company Dakota applicants: reputed company complies with applicable laws prohibiting smoking in and around places of employment. Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or reputed company employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Notice to Rhode reputed company applicants: reputed company complies with Rhode reputed company law prohibiting smoking in enclosed areas reputed company places of employment. reputed company is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode reputed company General Laws. Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR reputed company EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.

Originally posted on Himalayas

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