Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our ... Demonstrated competency in resource and project management, including budgeting, workforce planning ...
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our ... Demonstrated competency in resource and project management, including budgeting, workforce planning ...
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our ... Demonstrated competency in resource and project management, including budgeting, workforce planning ...
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our ... Demonstrated competency in resource and project management, including budgeting, workforce planning ...
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our ... Demonstrated competency in resource and project management, including budgeting, workforce planning ...
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our ... Demonstrated competency in resource and project management, including budgeting, workforce planning ...
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our ... Demonstrated competency in resource and project management, including budgeting, workforce planning ...
Assistant Director Clinical Regulatory Operations Hybrid role (3 days/week in office) at our ... Demonstrated competency in resource and project management, including budgeting, workforce planning ...
As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key role in ... Participate in monitor visits, QA/QC projects, site-level audits, and other quality activities ...
Quick apply
As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key role in ... Participate in monitor visits, QA/QC projects, site-level audits, and other quality activities ...
The Associate Director, Global Regulatory Affairs Project Management is an integral part of the ... Clinical, Safety, Biostatistics, CMC / Pharmaceutical Development and Manufacturing, etc. and ...
The Associate Director, Global Regulatory Affairs Project Management is an integral part of the ... Clinical, Safety, Biostatistics, CMC / Pharmaceutical Development and Manufacturing, etc. and ...
Position We are seeking an experienced Associate Director, Clinical Regulatory, to manage our ... Identify and assess regulatory risks associated with projects and proactively propose solutions to ...
Position We are seeking an experienced Associate Director, Clinical Regulatory, to manage our ... Identify and assess regulatory risks associated with projects and proactively propose solutions to ...
Project manages regulatory submissions from initiation through submission, supporting the ... Experience with complex oncology clinical trial designs (e.g., combination studies, multi-cohort ...
Project manages regulatory submissions from initiation through submission, supporting the ... Experience with complex oncology clinical trial designs (e.g., combination studies, multi-cohort ...
$134K - $162K/yr
Experience with all phases of clinical development * Demonstrable proficiency in project timeline ... Manager, Regulatory Affairs Project Management #J-18808-Ljbffr
$134K - $162K/yr
Experience with all phases of clinical development * Demonstrable proficiency in project timeline ... Manager, Regulatory Affairs Project Management #J-18808-Ljbffr
Manager, Regulatory Affairs Project Management Indianapolis - RayzeBio - IN R1605576
Indianapolis, IN · On-site
$134K - $162K/yr
Experience with all phases of clinical development * Demonstrable proficiency in project timeline ... Manager, Regulatory Affairs Project Management #J-18808-Ljbffr
Manager, Regulatory Affairs Project Management Indianapolis - RayzeBio - IN R1605576
Indianapolis, IN · On-site
$134K - $162K/yr
Experience with all phases of clinical development * Demonstrable proficiency in project timeline ... Manager, Regulatory Affairs Project Management #J-18808-Ljbffr
As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key role in ... Participate in monitor visits, QA/QC projects, site-level audits, and other quality activities ...
Quick apply
As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key role in ... Participate in monitor visits, QA/QC projects, site-level audits, and other quality activities ...
As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key role in ... Participate in monitor visits, QA/QC projects, site-level audits, and other quality activities ...
Quick apply
As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key role in ... Participate in monitor visits, QA/QC projects, site-level audits, and other quality activities ...
This role blends deep regulatory expertise with advanced project management skills, driving ... Build partnerships with senior stakeholders and cross-functional teams (clinical, medical, safety ...
This role blends deep regulatory expertise with advanced project management skills, driving ... Build partnerships with senior stakeholders and cross-functional teams (clinical, medical, safety ...
Clinical Regulatory Writer, Associate Director / Manager
Boston, MA · On-site
$133K - $199K/yr
Our team provides expert communications leadership to drug projects, authoring strategically important clinical-regulatory documents that align with project strategies and regulatory requirements. We ...
Clinical Regulatory Writer, Associate Director / Manager
Boston, MA · On-site
$133K - $199K/yr
Our team provides expert communications leadership to drug projects, authoring strategically important clinical-regulatory documents that align with project strategies and regulatory requirements. We ...
This role blends deep regulatory expertise with advanced project management skills, driving ... Build partnerships with senior stakeholders and cross-functional teams (clinical, medical, safety ...
This role blends deep regulatory expertise with advanced project management skills, driving ... Build partnerships with senior stakeholders and cross-functional teams (clinical, medical, safety ...
$130K - $140K/yr
Act as a dedicated clinical evaluation project manager, driving a coherent clinical evidence strategy throughout the product life cycle and aligning with marketing, regulatory, clinical research, and ...
New
$130K - $140K/yr
Act as a dedicated clinical evaluation project manager, driving a coherent clinical evidence strategy throughout the product life cycle and aligning with marketing, regulatory, clinical research, and ...
New
Sr. Staff Clinical Regulatory Scientist
Allendale, NJ · On-site +1
$130K - $140K/yr
Act as a dedicated clinical evaluation project manager, driving a coherent clinical evidence strategy throughout the new product development cycle and aligning with marketing, regulatory, clinical ...
Sr. Staff Clinical Regulatory Scientist
Allendale, NJ · On-site +1
$130K - $140K/yr
Act as a dedicated clinical evaluation project manager, driving a coherent clinical evidence strategy throughout the new product development cycle and aligning with marketing, regulatory, clinical ...
$110K - $146K/yr
Overview Reporting directly to the Yale Cancer Center (YCC) Clinical Trials Office (CTO) Director ... Capable of leading multiple projects within multidisciplinary environments at the same time.
$110K - $146K/yr
Overview Reporting directly to the Yale Cancer Center (YCC) Clinical Trials Office (CTO) Director ... Capable of leading multiple projects within multidisciplinary environments at the same time.
$134K - $162K/yr
Experience with all phases of clinical development * Demonstrable proficiency in project timeline ... Manager, Regulatory Affairs Project Management #J-18808-Ljbffr
$134K - $162K/yr
Experience with all phases of clinical development * Demonstrable proficiency in project timeline ... Manager, Regulatory Affairs Project Management #J-18808-Ljbffr
Manager, Regulatory Affairs Project Management Indianapolis - RayzeBio - IN R1605576 Posted a day ag
Indianapolis, IN · On-site
$134K - $162K/yr
Experience with all phases of clinical development * Demonstrable proficiency in project timeline ... Manager, Regulatory Affairs Project Management #J-18808-Ljbffr
Manager, Regulatory Affairs Project Management Indianapolis - RayzeBio - IN R1605576 Posted a day ag
Indianapolis, IN · On-site
$134K - $162K/yr
Experience with all phases of clinical development * Demonstrable proficiency in project timeline ... Manager, Regulatory Affairs Project Management #J-18808-Ljbffr
Clinical Regulatory Project Assistant information
See salary details
$11.54 - $13.11
1% of jobs
$13.11 - $14.69
5% of jobs
$14.69 - $16.26
15% of jobs
$16.57 is the 25th percentile. Wages below this are outliers.
$16.26 - $17.83
20% of jobs
The median wage is $18.86 / hr.
$17.83 - $19.41
14% of jobs
$19.41 - $20.98
13% of jobs
$20.98 - $22.55
7% of jobs
$22.60 is the 75th percentile. Wages above this are outliers.
$22.55 - $24.13
8% of jobs
$24.13 - $25.70
9% of jobs
$25.70 - $27.27
4% of jobs
$27.27 - $28.85
3% of jobs
$11
$20
$28
How much do clinical regulatory project assistant jobs pay per hour?
What are popular job titles related to Clinical Regulatory Project Assistant jobs?
For Clinical Regulatory Project Assistant jobs, the most frequently searched job titles are:

Assistant Director Clinical Regulatory Operations
Spokane, WA • Hybrid
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 20 hours ago
Key responsibilities
Leads a clinical regulatory operations team to ensure compliance with CMS, state, NCQA, Privacy, and contractual requirements.
Partners with stakeholders to identify, interpret, and operationalize regulatory requirements and establish monitoring and remediation frameworks.
Collaborates with clinical business owners and cross-functional teams to align processes, improve operational efficiency, and support regulatory compliance.
Cambia Health Solutions rating
8.4
Based on 32 frontline employees who took The Breakroom Quiz
Job description
Assistant Director Clinical Regulatory Operations
Hybrid role (3 days/week in office) at our Burlington, Renton, Spokane, Vancouver, Portland, Medford, Salt Lake City, Boise, Lewiston, Fargo offices.
Preference will be given to current employees and candidates who reside within a commutable distance from our Salt Lake City, Boise, Fargo and Lewiston offices or who are willing to relocate.
Build a career with purpose. Join our Cause to create a person-focused and economically sustainable health care system.
Who We Are Looking For:
Every day, Cambia's dedicated team of Clinical leaders are living our mission to make health care easier and lives better. As a member of the Transformation, Quality, and Learning team, our Assistant Director Clinical Regulatory Operations leads a clinical regulatory operations team that serves as a strategic partner to HSO clinical business leaders - enabling the pursuit of improved affordability, operational efficiency, quality, and member experience within a framework of regulatory compliance. This role ensures all Health Services Operations (HSO) operate in compliance with CMS, state, NCQA, Privacy, and contractual requirements - while applying improvement science to advance operations toward sustainable excellence. The role will partner with Cambia regulatory stakeholders and clinical business owners to identify and operationalize evolving requirements, establish scalable monitoring and remediation frameworks, and facilitate operational simplification by aligning processes across teams and lines of business where appropriate - all in service of creating a person-focused health care experience.
As a people leader, you are willing to learn and grow, understanding that leadership is a craft that is continuously honed as you support your team and the lives that depend upon us.
Ready to lead regulatory excellence at the intersection of compliance and innovation during health care's most transformative era? Want to shape how multiple health systems work together-building the compliance framework that enables better care for thousands of members? Then this role may be the perfect fit.
What You Bring to Cambia:
Qualifications:
Bachelor's degree in Healthcare Administration, Nursing, Public Health, or a related field (Master's preferred)
5 years of leadership experience
7 years of health insurance or managed care experience focused on regulatory compliance, quality management, or clinical operations - or an equivalent combination of education and experience
Skills and Attributes:
Demonstrated knowledge of CMS, state, NCQA, HIPAA/Privacy, and managed care contract compliance requirements as applied across Utilization Management & Appeals, Care Management, Pharmacy, and Payment Integrity.
Ability to interpret complex regulatory requirements and translate them into clear, actionable operational guidance for diverse audiences.
Demonstrated competency in designing and executing compliance monitoring, auditing, and reporting programs in a health plan or managed care environment.
Demonstrated knowledge and application of improvement science methodologies (e.g., PDSA, Lean, Six Sigma), with the ability to drive operational improvement beyond compliance monitoring.
Demonstrated ability to analyze and align operational processes across multiple teams and lines of business to achieve standardization, simplification, and scalability.
Experience leading cross-functional regulatory implementation efforts in collaboration with clinical operations, legal, compliance, and regulatory affairs.
Ability to identify compliance gaps, conduct root cause analysis, and lead data-driven remediation across operational teams.
Experience leveraging automation, data analytics, and technology to enhance compliance monitoring and program effectiveness; familiarity with dashboard development or workflow automation preferred.
Demonstrated competency in resource and project management, including budgeting, workforce planning, and managing to deliverables.
Ability to develop and lead teams across multiple locations or remote environments, including hiring, goal setting, coaching, and development.
Strong written and verbal communication skills, including regulatory memos, executive reporting, and presentations.
Experience writing policies and procedures and developing monitoring and auditing tools.
Experience with AI tools and technologies to enhance productivity and decision-making highly desired.
What You Will Do at Cambia:
Partners with Regulatory Affairs, Quality, Legal, Compliance, and clinical business owners to identify, interpret, and operationalize new and evolving regulatory requirements across all HSO program areas (Utilization Management & Appeals, Care Management, Pharmacy, Payment Integrity). Serves as strategic partner to HSO clinical leaders, enabling improved affordability, operational efficiency, quality, and member experience within regulatory guardrails.
Facilitates operational simplification by systematically comparing and aligning processes across teams and lines of business-standardizing where appropriate to reduce redundancy, scale consistent compliance practices, and streamline operations using improvement science methodologies.
Designs and executes regulatory compliance programs using structured improvement models (PDSA, Lean, Six Sigma) to drive program maturity and advance operations toward embedded operational excellence. Continuously evaluates program efficiency to streamline processes, eliminate waste, and optimize resources.
Establishes and continuously improves audit and monitoring processes, incorporating automation, dashboards, and real-time reporting in partnership with data, analytics, and technology teams. Develops compliance reporting frameworks leveraging automation and data visualization to provide leadership with timely, actionable insights on compliance status, risk exposure, and program performance.
Manages corrective action plans from internal monitoring, external audits, and accreditation surveys-applying root cause analysis to address systemic drivers and ensure sustainable remediation. Collaborates with Cambia Regulatory stakeholders to identify emerging compliance trends, detect risk areas, and recommend proactive mitigation strategies while ensuring legislative, regulatory, and accreditation changes are implemented within required timeframes.
Leads NCQA accreditation readiness activities including gap assessments, mock audits, and submission preparation. Oversees the HSO Rapid Resolution Team managing complex member escalation cases with systematic root cause analysis and trend monitoring. Oversees the Clinical Review Inter-rater Reliability program ensuring evidence-based, objective reviews with structured calibration processes, statistically valid sampling, and performance benchmarks aligned with NCQA, URAC, and industry best practices.
Handles all management responsibilities including performance reviews, development, hiring, coaching, and retention. Manages department budget, authorizes expenditures, monitors workforce allocation, and oversees project plans. Establishes long-term department goals in conjunction with division leadership and acts as liaison between HSO program areas and enterprise stakeholders.
As a member of our strong leadership community, you will provide direction to your team, engage them towards common goals and create a positive experience that helps people flourish.
FTEs Supervised
30 FTEs
#LI-Hybrid
Pay ranges vary based on the candidate's work location. The expected hiring range depends on skills, experience, education, and training; relevant licensure / certifications; and performance history.
Oregon, Washington, Utah, and Idaho:The expected hiring range is $136,000 - $184,000, the full salary range is$128,000 - $208,000 and the bonus target is20%.
North Dakota:The full salary range is $113,780 - $187,737 and the bonus target is15%.
About Cambia
Working at Cambia means being part of a purpose-driven, award-winning culture built on trust and innovation anchored in our 100+ year history. Our caring and supportive colleagues are some of the best and brightest in the industry, innovating together toward sustainable, person-focused health care. Whether we're helping members, lending a hand to a colleague or volunteering in our communities, our compassion, empathy and team spirit always shine through.
Why Join the Cambia Team?
At Cambia, you can:
- Work alongside diverse teams building cutting-edge solutions to transform health care.
- Earn a competitive salary and enjoy generous benefits while doing work that changes lives.
- Grow your career with a company committed to helping you succeed.
- Give back to your community by participating in Cambia-supported outreach programs.
- Connect with colleagues who share similar interests and backgrounds through our employee resource groups.
We believe a career at Cambia is more than just a paycheck - and your compensation should be too. Our compensation package includes competitive base pay as well as a market-leading 401(k) with a significant company match, bonus opportunities and more.
In exchange for helping members live healthy lives, we offer benefits that empower you to do the same. Just a few highlights include:
- Medical, dental and vision coverage for employees and their eligible family members, including mental health benefits.
- Annual employer contribution to a health savings account.
- Generous paid time off varying by role and tenure in addition to 10 company-paid holidays.
- Market-leading retirement plan including a company match on employee 401(k) contributions, with a potential discretionary contribution based on company performance (no vesting period).
- Up to 12 weeks of paid parental time off (eligibility requires 12 months of continuous service with Cambia immediately preceding leave).
- Award-winning wellness programs that reward you for participation.
- Employee Assistance Fund for those in need.
- Commute and parking benefits.
Learn more about our benefits.
We are happy to offer work from home options for most of our roles. To take advantage of this flexible option, we require employees to have a wired internet connection that is not satellite or cellular and internet service with a minimum upload speed of 5Mb and a minimum download speed of 10 Mb.
As part of our security requirements, new hires will need access to a personal mobile device to set up Multi-Factor Authentication (MFA) upon joining the company. MFA is an important layer of protection for accessing Cambia systems and is required for all employees.
We are an Equal Opportunity employer dedicated to a drug and tobacco-free workplace. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, age, sex, sexual orientation, gender identity, disability, protected veteran status or any other status protected by law. A background check is required.
If you need accommodation for any part of the application process because of a medical condition or disability, please email CambiaCareers@cambiahealth.com. Information about how Cambia Health Solutions collects, uses, and discloses information is available in our Privacy Policy.
What Cambia Health Solutions employees say
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About Cambia Health Solutions
Sourced by ZipRecruiter
Industry
Health care and social assistance
Company size
1,001 - 5,000 Employees
Headquarters location
Portland, OR, US
Year founded
1996