Regulatory Specialist designs, directs and facilitates implementation of effective systems to ... Associate or Baccalaureate in Nursing. Masters in Nursing or Business Degree preferred. * Licensure ...
Regulatory Specialist designs, directs and facilitates implementation of effective systems to ... Associate or Baccalaureate in Nursing. Masters in Nursing or Business Degree preferred. * Licensure ...
Regulatory Specialist designs, directs and facilitates implementation of effective systems to ... Associate or Baccalaureate in Nursing. Masters in Nursing or Business Degree preferred. * Licensure ...
Regulatory Specialist designs, directs and facilitates implementation of effective systems to ... Associate or Baccalaureate in Nursing. Masters in Nursing or Business Degree preferred. * Licensure ...
Regulatory Specialist designs, directs and facilitates implementation of effective systems to ... Associate or Baccalaureate in Nursing. Masters in Nursing or Business Degree preferred. * Licensure ...
Regulatory Specialist designs, directs and facilitates implementation of effective systems to ... Associate or Baccalaureate in Nursing. Masters in Nursing or Business Degree preferred. * Licensure ...
Clinical Regulatory Writer, Associate Director / Manager
Boston, MA · On-site
$133K - $199K/yr
Clinical Regulatory Writer, Associate Director / Manager Location: Boston, MA OR Gaithesrburg, MD- Hybrid (3 days onsite) Introduction to role: Are you ready to be part of the solution, turning drug ...
Clinical Regulatory Writer, Associate Director / Manager
Boston, MA · On-site
$133K - $199K/yr
Clinical Regulatory Writer, Associate Director / Manager Location: Boston, MA OR Gaithesrburg, MD- Hybrid (3 days onsite) Introduction to role: Are you ready to be part of the solution, turning drug ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
JOB SUMMARY The Research Regulatory Associate I supports clinical research activities through the development of protocol-specific documents and reports for research activities from initial ...
Quick apply
JOB SUMMARY The Research Regulatory Associate I supports clinical research activities through the development of protocol-specific documents and reports for research activities from initial ...
Solid knowledge of Regulatory Agency organizations. Applies gained knowledge and experience to ... Clinical Recruiter 732-844-8725 indu @irionline.com
Solid knowledge of Regulatory Agency organizations. Applies gained knowledge and experience to ... Clinical Recruiter 732-844-8725 indu @irionline.com
JOB SUMMARY The Research Regulatory Associate I supports clinical research activities through the development of protocol-specific documents and reports for research activities from initial ...
JOB SUMMARY The Research Regulatory Associate I supports clinical research activities through the development of protocol-specific documents and reports for research activities from initial ...
JOB SUMMARY The Research Regulatory Associate I supports clinical research activities through the development of protocol-specific documents and reports for research activities from initial ...
JOB SUMMARY The Research Regulatory Associate I supports clinical research activities through the development of protocol-specific documents and reports for research activities from initial ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
We are seeking a detail-oriented Regulatory Associate to join our Regulatory Affairs team. In this ... Prepare, review, and submit regulatory documentation for clinical trial applications, product ...
We are seeking a detail-oriented Regulatory Associate to join our Regulatory Affairs team. In this ... Prepare, review, and submit regulatory documentation for clinical trial applications, product ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
In this role, you will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials under the leadership of the Cancer Center Associate Director of ...
USA_Regulatory Associate - Level 3
Warren, NJ · On-site
$49.15/hr
Job Title: USA_Regulatory Associate - Level 3 Location: Warren, NJ Type: 12-month contract ... Clinical
Quick apply
USA_Regulatory Associate - Level 3
Warren, NJ · On-site
$49.15/hr
Job Title: USA_Regulatory Associate - Level 3 Location: Warren, NJ Type: 12-month contract ... Clinical
... for a Regulatory Associate. About the Opportunity This position examines, evaluates, and ... Working in a clinical setting and/or experience working in clinical trials. * Any equivalent ...
... for a Regulatory Associate. About the Opportunity This position examines, evaluates, and ... Working in a clinical setting and/or experience working in clinical trials. * Any equivalent ...
About the Role The Associate Director, Regulatory Affairs - Nonclinical Development is a strategic regulatory leader specializing in nonclinical drug development. This role is responsible for guiding ...
About the Role The Associate Director, Regulatory Affairs - Nonclinical Development is a strategic regulatory leader specializing in nonclinical drug development. This role is responsible for guiding ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Olyphant, PA · On-site
About the Role The Associate Director, Regulatory Affairs - Nonclinical Development is a strategic regulatory leader specializing in nonclinical drug development. This role is responsible for guiding ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Olyphant, PA · On-site
About the Role The Associate Director, Regulatory Affairs - Nonclinical Development is a strategic regulatory leader specializing in nonclinical drug development. This role is responsible for guiding ...
The Regulatory Associate will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials as well as provide support and backup for other DOTs as ...
The Regulatory Associate will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials as well as provide support and backup for other DOTs as ...
Clinical Regulatory Associate information
See salary details
$12.74 - $16.61
3% of jobs
$16.61 - $20.48
18% of jobs
$21.24 is the 25th percentile. Wages below this are outliers.
$20.48 - $24.34
20% of jobs
The median wage is $26.69 / hr.
$24.34 - $28.21
15% of jobs
$28.21 - $32.08
11% of jobs
$32.08 - $35.95
4% of jobs
$39.24 is the 75th percentile. Wages above this are outliers.
$35.95 - $39.82
5% of jobs
$39.82 - $43.68
8% of jobs
$43.68 - $47.55
6% of jobs
$47.55 - $51.42
6% of jobs
$51.42 - $55.29
3% of jobs
$12
$31
$55
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Clinical Regulatory Specialist
Columbus, OH • On-site
Other
Medical, Dental, Vision, Retirement, PTO
This job post has expired 1 day ago. Applications are no longer accepted.
Trinity Health Mid-Atlantic rating
7.6
Based on 40 frontline employees who took The Breakroom Quiz
Job description
Employment Type: Full time Shift:
Why Mount Carmel?With five hospitals, over 60 free‑standing outpatient clinics, a college of nursing, a Medicare Advantage plan, and extensive outreach and community wellness programs, Mount Carmel Health System serves more than a million patients in central Ohio each year, and we've been a pillar of this community for more than 130 years. As a proud member of Trinity Health, one of the nation's largest Catholic healthcare delivery systems, our network of caring spans 22 states, 94 hospitals, and 133,000 colleagues nationwide. We know that exceptional patient care starts with taking care of our colleagues, so we invest in great people and all that we ask in return is that you come to work ready to make a difference and do the right thing.
What we offer:- Competitive compensation and benefits packages including medical, dental, and vision coverage
- Retirement savings account with employer match starting on day one
- Generous paid time off programs
- Employee recognition incentive program
- Tuition/professional development reimbursement
- Relocation assistance (geographic restrictions apply)
- Discounted tuition and enrollment opportunities at the Mount Carmel College of Nursing
The nation's 14th largest city, Columbus, Ohio is one of the fastest growing major metropolitan areas in the Midwest – ranked #1 for population growth, #1 for job growth, #1 for wage growth, and #1 real estate market. And with a vibrant blend of professional sports, world‑class attractions, creative cuisines, and a flourishing music and arts scene, you'll never be asked to find yourself wanting for entertainment and experiences to call your own in Columbus. Learn more at www.experiencecolumbus.com!
About the job:Regulatory Specialist designs, directs and facilitates implementation of effective systems to evaluate compliance and assure continuous accreditation and regulatory compliance. Scope includes Mount Carmel owned and affiliated entities managed by Mount Carmel Health System.
What you’ll do:- Accountable for the preparation and support of wholly owned facilities, relative to regulatory and licensure compliance.
- Responsibility includes multi‑site locations and requires travel to each of the facilities.
- Assists in scheduled/unannounced surveys by regulatory agencies.
- Assists in evaluation of regulatory compliance and operations from a process perspective across departments and/or multiple service areas.
- Facilitates and uses change principles to accomplish regulatory compliance and continuous survey readiness.
- Serves as a role model to demonstrate openness to new ways of thinking.
- Facilitates communication both external and internal to affiliated organizations as necessary to meet regulatory requirements.
- Advises on matters regarding regulatory requirements in the development and implementation of organization plans or activities.
- Serves as a liaison with external agencies (CMS, ODH, JCAHO, etc) as well as Trinity Health System.
- Provides consultation for practical and reasonable interpretations of regulatory requirements.
- Assists in organizational planning for integration of regulatory requirements into daily work activities.
- Manages medical staff dynamics to facilitate effective discussions and participation in regulatory compliance activities.
- Works with diverse groups, settings and varied kinds of complexities.
- Develops and/or assists in conducting educational programs or in‑services related to regulatory requirements as needed or requested by the organization.
- Serves as project manager as needed for organizational endeavors.
- Provides, as requested, consulting services to non‑MCHS owned health care entities for purposes of building targeted relationships.
- Tailors implementation approaches to different sites and processes.
- Assists managers in identifying solutions to challenging regulatory issues.
- Provides assistance to the Privacy Officer as needed.
- Serves as the Chairperson for the MCHS Administrative Policy Team.
- Serves as the administrative liaison with organ procurement agencies.
- Participates in activities which promote own professional growth and development.
- Education: Associate or Baccalaureate in Nursing. Masters in Nursing or Business Degree preferred.
- Licensure / Certification: Registered Nurse with a current Ohio License
- Experience: Minimum of five (5) years recent healthcare practice. Clinical and management experience preferred.
- Effective Communication Skills
- Broad based clinical or management leadership experience with knowledge of complex systems and systems change with demonstrated success in tactical and analytical thinking.
- Knowledge of performance improvement systems and process thinking principles and designs.
- Current knowledge of regulatory and accrediting requirements.
- Proficient computer, written and verbal communications skills; excellent presentation skills with ability to relate effectively to physicians, all levels of the organization and employees in a flexible and adaptive fashion.
- Innovative, self directed, flexible, and collaborative.
- Readily accepts change and influences organizational change.
- Understands and applies group process skills.
- Demonstrates a high tolerance for ambiguity.
- Able to incorporate standards interpretation into day‑to‑day operations.
- Able to mobilize action; interactive.
Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person‑centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.
Mount Carmel and all its affiliates are proud to be equal opportunity employers. We do not discriminate on the basis of race, gender, religion, physical disability or any other classification protected under local, state or federal law.
Trinity Health is one of the largest not‑for‑profit, faith‑based health care systems in the nation. Together, we’re 121,000 colleagues and nearly 36,500 physicians and clinicians caring for diverse communities across 27 states. Nationally recognized for care and experience, our system includes 101 hospitals, 126 continuing care locations, the second largest PACE program in the country, 136 urgent care locations, and many other health and well‑being services. Based in Livonia, Michigan, in fiscal year 2023, we invested 1.5 billion in our communities through charity care and other community benefit programs. For more information, visit http://www.trinity-health.org.
You can also follow Trinity Health on LinkedIn.
What Trinity Health Mid-Atlantic employees say
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Benefits
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About Trinity Health Mid Atlantic
Sourced by ZipRecruiter
Company size
1 - 10 Employees
Headquarters location
Newtown Square, PA, US
Year founded
2018