Assistant Director, Regulatory

3 weeks ago


San Francisco, United States Metropolitan Transportation Commission Full time

Details

**Posted**: 22-Apr-24

**Location**: San Francisco, California

**Type**: Full Time

**Salary**: $164,940.67 - $219,760.94 /yr

**Categories**:

- Operations

**Years of Experience**:

- Less than 2

**Metropolitan Transportation Commission**

**San Francisco, CA**

**Assistant Director, Regulatory & Risk Management**

**$164,940.67 - $219,760.94 Annually**

**Remote Employment: Flexible/Hybrid**

**THIS JOB POSTING WILL REMAIN OPEN UNTIL A QUALIFIED POOL OF APPLICANTS IS ESTABLISHED**

**FIRST REVIEW OF APPLICATIONS WILL BE ON WEDNESDAY, MAY 1, 2024**

**IF YOU ARE INTERESTED, PLEASE APPLY IMMEDIATELY**

**First round interviews tentatively scheduled for Thursday, May 9, 2024**

Be ready to rethink your assumptions about the public sector. Dedicated and motivated colleagues? Beautiful, high amenity building for on-site work and collaboration? Flexible schedules and hybrid work options? Yes, yes, and yes

The Assistant Director (AD), Regulatory and Risk Management at the Metropolitan Transportation Commission (MTC) will report to the Director of the Facilities and Contract Services (FCS) section and will closely collaborate with Executive Office and Office of General Counsel (OGC) staff to implement the new Regulatory and Risk Management unit within FCS.

The primary duties for the Assistant Director, Regulatory and Risk Management position will consist of managing and overseeing the insurance program, risk management, and regulatory compliance with grant, state, local, federal requirements, including but not limited to, the Americans with Disabilities Act (ADA), accessibility, Title VI, Limited English Proficiency (LEP), Disadvantaged Business Enterprise (DBE), Small Business Enterprise (SBE), and third-party labor compliance/prevailing wage. The AD Regulatory and Risk Management will also undertake strategic initiatives, administrative and operational systems analyses, including project management/coordination of the agency’s insurance/risk management program, claims, primary oversight for audit related to compliance and contracts, and performs other duties as assigned. The assigned duties will range in difficulty and complexity, up to and including supervisory duties.

All employees at MTC are classified as Disaster Service Workers.

**SKILLS AND ABILITIES**
- Previous experience in management of local, state, and/or federal regulatory programs, civil rights, risk, and liability claims programs and operations.
- Principles, policies, practices, and procedures of civil rights program requirements, economic diversity and inclusion programs including, but not limited to, DBE/SBE program development and/or administration, Title VI, ADA, risk management programs, policies, and procedures.
- Ability to monitor and report on program compliance and performance.
- Excellent oral, written, and presentation skills that allow for clear and concise communication.
- Work effectively under pressure and meet critical deadlines.
- Establish and maintain effective working relationships.
- Previous management experience developing and implementing goals, objectives, policies, and procedures related to risk management, and/or civil rights programs.

**MINIMUM QUALIFICATIONS**

An appropriate combination of education and experience that has provided the required knowledge, skills and abilities is qualifying. A typical way of obtaining the required qualifications is:
**Experience**: Four years of increasingly responsible experience in an appropriate field related to the area of assignment.

**(A Master’s degree in an appropriate discipline and three years of relevant experience is an alternative minimum qualification.)

**Preferred Qualifications**:
**Education**: Equivalent to a Bachelor's degree from an accredited four-year college or university in Business Administration, Public Administration, management, or a related field.

**Experience**: Five (5) years of verifiable and increasingly responsible experience in managing and administering civil rights or similar programs, risk, liability claims programs and operations. Previous supervisory experience is also recommended but not required.

**License/Certificate**: Possession of a valid California Class C driver's license and a safe driving record, or the ability to provide alternate transportation which is approved by the appointing authority.

**ESSENTIAL DUTIES AND RESPONSIBILITIES**

Specific duties and responsibilities include, but are not limited to, directly performing, or overseeing staff performing the following:
**Risk Management**
- Provide technical expertise to develop a risk management program; perform and coordinate a variety of standard and complex professional administrative, operational, and risk management activities; plan, organize, monitor, integrate, and evaluate work performed by consultants and insurance brokers.
- Strategize risk management approaches; research, analyze, and recommend approaches for identifying, managing, and mitigatin



  • San Francisco, United States Metropolitan Transportation Commission Full time

    **DESCRIPTION**: **THIS JOB POSTING WILL REMAIN OPEN UNTIL A QUALIFIED POOL OF APPLICANTS IS ESTABLISHED** **FIRST REVIEW OF APPLICATIONS WILL BE ON WEDNESDAY, MAY 1, 2024** **IF YOU ARE INTERESTED, PLEASE APPLY IMMEDIATELY** **First round interviews **tentatively **scheduled for Thursday, May 9, 2024** - ._ - Be ready to rethink your assumptions about...


  • San Francisco, United States Meet Recruitment Full time

    Meets clinical-stage biopharmaceutical client based in the Bay Area is seeking a highly motivated individual to join their growing regulatory affairs group. The Associate Director / Director, Regulatory Affairs will work closely with the Regulatory Affairs team and other departments to develop and implement regulatory strategies for the company's rare...


  • San Francisco, United States Financial Industry Regulatory Authority , Inc. Full time

    The Senior Regulatory Operations Analyst is an advanced-level professional position responsible for a wide range of tasks in support of various regulatory compliance functions in Market Regulation and Transparency Services (MRTS), including those related to managing conflicts of interest-related compliance issues and inquiries and maintaining department-wide...


  • San Francisco, United States BioLink 360 Full time

    Company Location: Bay Area Comp: 150K-220K Position Reports to: VP of Regulatory and Quality Director of Regulatory Affairs -San Francisco We are seeking a highly motivated and experienced Senior Director of Regulatory Affairs for a Medical Device Orthopedic Portfolio. This person will lead interactions with regulatory agencies globally and help develop &...


  • San Francisco, United States Trebla Talent Full time

    Role: Senior Director, Regulatory Operations Bay Area Company Description: This is a next-generation cell therapy biotech developing treatments for chronic autoimmune disorders. After four Investigational New Drug (IND) milestones in the past year alone, the team is expecting significant clinical activity, and an explosive hiring period across the...


  • South San Francisco, California, United States Andromeda Surgical Full time

    Company DescriptionAt Andromeda Surgical, we are developing autonomous robots with the goal of making surgical procedures safer, easier, and more efficient. We are starting with a urologic procedure that has superior outcomes but a steep learning curve that has limited its adoption. Our mission is to elevate every surgeon to world expert level, empowering...


  • South San Francisco, United States Maze Therapeutics Full time

    The Position: Join our dynamic Regulatory Affairs team as a Director, Regulatory Affairs, where you will be the driving force behind our development programs from preclinical candidate designation through drug approval. We are looking for a strategic thinker and regulatory expert to provide leadership and guidance. As the Global Program Lead, you will...


  • South San Francisco, United States Cytokinetics Full time

    Reporting to the Senior Director, Regulatory Affairs, the Associate Director of Regulatory Affairs leads regulatory support for assigned programs to ensure sound regulatory planning and tactical implementation of US and international development strategies. **Responsibilities** - Formulate regulatory strategies, with supervisor oversight, based on current...


  • South San Francisco, United States Maze Therapeutics Full time

    Job DescriptionJob DescriptionThe Position:Join our dynamic Regulatory Affairs team as a Director, Regulatory Affairs, where you will be the driving force behind our development programs from preclinical candidate designation through drug approval. We are looking for a strategic thinker and regulatory expert to provide leadership and guidance. As the Global...


  • San Francisco, United States Pfizer Full time

    Work Location Assignment: Onsite/Hybrid Why Patients Need You We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and...


  • San Francisco, United States Pfizer Full time

    Work Location Assignment:Onsite/Hybrid Why Patients Need You We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and theever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise...


  • South San Francisco, United States Remegen Biosciences, Inc. Full time

    Job DescriptionJob DescriptionORGANIZATIONRemeGen Biosciences is a biopharmaceutical company, focusing on the discovery and development of innovative medicines for the treatment of cancer and autoimmune diseases, based in South San Francisco, California, and Rockville, Maryland. By leveraging our deep insights into oncology and immunology, advanced protein...


  • San Francisco, California, United States Nobell Foods Full time

    Nobell Foods is creating cheese and other dairy products from plant-derived dairy proteins for the 99% of people who are unwilling to compromise on taste and price. Nobell is made up of a team of passionate scientists, explorers, and storytellers on a mission to radically change the way we make food, so its better for you, the animals and the planet. We are...


  • San Jose, United States Veranex, Inc. Full time

    Director or Senior Director, Regulatory Affairs San Jose, CA, USA Req #183 Thursday, May 2, 2024 Veranex is the only truly comprehensive, global, tech-enabled service provider dedicated to the medical technology industry. Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical...


  • San Diego, United States Avidity Biosciences Full time

    **Job Title**: Director, Regulatory Operations **Location**: Hybrid / Remote **Position type**: **FLSA**: Full time- Exempt**Department**: Regulatory Affairs **Strive to Bring a** Profound Difference to our Patients**: At Avidity Biosciences, we are passionate about the impact of every employee in realizing our vision of improving people’s lives by...


  • San Diego, California, United States Avidity Biosciences Full time

    Job Title:Director, Regulatory OperationsLocation:Hybrid / RemotePosition type:FLSA:Full time- ExemptDepartment:Regulatory AffairsStrive to Bring a Profound Difference to our Patients**:At Avidity Biosciences, we are passionate about the impact of every employee in realizing our vision of improving people's lives by delivering a new class of RNA...


  • San Francisco, United States Abdera Therapeutics Full time

    Abdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing healthy...


  • San Francisco, United States Abdera Therapeutics Full time

    Abdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing healthy...


  • San Carlos, United States Cargo Therapeutics Full time

    The **Director, Regulatory Affairs** will be responsible for providing global regulatory leadership in support of the development, registration, and lifecycle management of CARGO’s oncology products. They will ensure effective achievement of regulatory/business objectives across teams, within the department, and at the corporate level. The Director will...


  • South San Francisco, United States Abdera Therapeutics Full time

    Job DescriptionJob DescriptionSalary Range :  US$ 200K - $270KWho we are Abdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of...