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Associate Director Study Abroad Jobs in Riverside, CA

Learn more at JOB SUMMARY This Associate Director, Clinical Research will be leading a team of ... Leads study design to develop appropriate clinical trials to meet the clinical evidence needs;

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Associate Director Study Abroad information

See Riverside, CA salary details

$46.9K

$133.9K

$242.6K

How much do associate director study abroad jobs pay per year?

As of Aug 5, 2026, the average yearly pay for associate director study abroad in Riverside, CA is $133,921.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $196,700.00 per year, depending on experience, location, and employer.

What is the difference between Associate Director Study Abroad vs Study Abroad Coordinator?

AspectAssociate Director Study AbroadStudy Abroad Coordinator
Required CredentialsBachelor's degree, often master's preferred; experience in international educationBachelor's degree; experience in student services or international programs
Work EnvironmentAdministrative offices, university departments, international officesStudent services offices, campus international programs
Employer & Industry UsageHigher education institutions, study abroad officesColleges, universities, study abroad program providers
Common Search & Comparison IntentUnderstanding leadership roles, responsibilities, and qualificationsEntry-level duties, program coordination, and student support

The Associate Director Study Abroad typically holds a higher-level position with leadership responsibilities, requiring more experience and advanced credentials. In contrast, the Study Abroad Coordinator focuses on program logistics and student support, often serving in an entry to mid-level role. Both roles are essential in international education but differ in scope, responsibilities, and seniority.

What are some common challenges faced by an associate director study abroad, and how can I prepare to address them?

As an Associate Director of Study Abroad, you may frequently encounter challenges such as managing complex international partnerships, ensuring student safety and well-being, and adapting to rapidly changing global circumstances. Effective communication and crisis management skills are essential, as you will need to coordinate with students, faculty, and overseas institutions. Staying current with international regulations and maintaining flexible problem-solving approaches will help you navigate these challenges successfully. Proactive planning and cultivating strong relationships across campus and with global partners can also support your success in this role.

What are the key skills and qualifications needed to thrive as an associate director study abroad?

To thrive as an Associate Director Study Abroad, you need expertise in international education, program management, and cross-cultural communication, typically supported by a master’s degree in a relevant field. Familiarity with study abroad management software, risk management protocols, and compliance regulations is important, as well as certifications like Forum on Education Abroad’s Professional Certification. Exceptional interpersonal skills, problem-solving abilities, and cultural sensitivity set candidates apart in this role. These skills ensure effective program administration, student support, and the successful navigation of complex international partnerships.

What does an associate director study abroad do?

An Associate Director of Study Abroad oversees the development, administration, and evaluation of study abroad programs at a college or university. Their responsibilities include managing staff, ensuring program compliance with institutional and governmental regulations, advising students, and collaborating with international partners. They also handle budgeting, risk management, and marketing for study abroad opportunities to maximize student participation and ensure program quality.
What job categories do people searching Associate Director Study Abroad jobs in Riverside, CA look for? The top searched job categories for Associate Director Study Abroad jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Associate Director Study Abroad jobs? Cities near Riverside, CA with the most Associate Director Study Abroad job openings:

Associate Director, Clinical Affairs

Becton, Dickinson and Company

Irvine, CA • On-site, Remote

Full-time

Re-posted 24 days ago


BD rating

7.3

Company rating: 7.3 out of 10

Based on 140 frontline employees who took The Breakroom Quiz

305th of 487 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

About the role:

This is a senior leadership role responsible for endtoend oversight of complex clinical studies and registries within a highly regulated environment. The role leads managers and teams across multiple largescale initiatives, partners closely with investigators, hospitals, CROs, and internal stakeholders, and ensures regulatory compliance, data integrity, and study execution from initiation through completion. Ideal candidates bring deep clinical operations experience, strong people leadership capability, and a proven ability to manage risk and deliver results across highimpact, crossfunctional programs.

Key responsibilities include:

  • Manage senior managers, managers, and professionals to oversee the work of multiple projects and/or initiatives and may have financial budget responsibilities.
  • Develop a robust talent development plan in alignment with functional growth strategies of the department.
  • Identify risk, develop and lead in the implementation of broad and more complex projects, initiatives and/or strategies which may include negotiations with internal and external parties.
  • Develop mitigation strategies, alternative solutions, resolve issues, etc. in collaboration with cross functional and/or matrix teams
  • Plan and direct complex activities with large scale or significant business impact with the accountability for successful completion of all deliverables including but not limited to:
  • Oversee the relationship management of physicians/investigators, other medical professionals, Research Organizations (CRO's), hospitals, research institutions and/or vendors
  • Ensure compliance to applicable regulatory requirements including safety reporting and device related complications through appropriate oversight
  • Oversee clinical studies/registries from initiation to completion, while ensuring study compliance and data completeness
  • Serve as a point of escalation for complex project issues (e.g., sponsor site interaction for IRBs, contract, and training)
  • Oversee the Clinical Affairs Trial Management Team during clinical trial cases with physicians, hospital staff and coordinators
  • Oversee the accuracy/effectiveness of device accountability

Required education and experience

  • Bachelor's Degree (preferably in life sciences)
  • At least 10 years of professional clinical research, clinical operations, or trial management in a regulated environment (Device, Pharma, or Clinical Research Operations).
  • Endtoend leadership experience of clinical studies/registries
  • At least 5 years of people management experience or leading sizeable cross functional teams
  • Experience overseeing complex, high-impact programs in regulated environment (medical device research required) industry sponsored researchpreferred
  • Demonstrated experience leading managers and senior managers across multiple concurrent projects or initiatives.
  • Strong risk assessment, mitigation planning, and issueresolution skills within complex, crossfunctional environments.
  • Experience overseeing clinical studies/registries from initiation through completion, ensuring compliance and data integrity.
  • Solid understanding of regulatory requirements, including safety reporting and devicerelated event oversight

Preferred qualifications:

  • Experience serving as an escalation point for IRB interactions, contracts, training, and complex study issues. (Institutional Review Board)
  • Background supporting clinical trial teams during live case support with physicians and hospital staff.
  • Familiarity with device accountability processes and oversight procedures.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

Optional Skills

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Primary Work LocationUSA CA - Irvine Laguna CanyonAdditional LocationsWork Shift

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

$175,800.00 - $281,300.00 USD Annual

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About BD

Sourced by ZipRecruiter

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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