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Clinical Research Director Jobs in Riverside, RI

micro1 AI

Director of Biostatistics

Brockton, MA · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

New Bedford, MA · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Providence, RI · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

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Clinical Research Director information

See Riverside, RI salary details

$10

$53

$114

How much do clinical research director jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical research director in Riverside, RI is $53.33, according to ZipRecruiter salary data. Most workers in this role earn between $31.83 and $70.29 per hour, depending on experience, location, and employer.

What does a clinical research director do?

A clinical research director manages medical or pharmaceutical research projects. In this role, you may oversee a research department at a university or medical facility. Your specific job duties vary, depending on the type of project you work on, but your general responsibilities include overseeing the planning stages of each research project or clinical trial, discussing outcomes and expectations with researchers, making sure that research staff members provide the proper care to participants in the trial or research project, and ensuring that data is documented properly. Clinical research directors also hire and train new staff members and check that the project follows all governmental and industry guidelines.

What are the responsibilities of a clinical research director?

A Clinical Research Director oversees the planning, coordination, and management of clinical trials and research projects within healthcare or pharmaceutical organizations. They ensure studies comply with regulatory requirements, establish research protocols, manage budgets, and supervise research teams. Additionally, they collaborate with stakeholders, analyze data, and ensure that clinical trials are conducted ethically and efficiently to advance medical knowledge and patient care.

What are the key skills and qualifications needed to thrive as a clinical research director, and why are they important?

To thrive as a Clinical Research Director, you need advanced knowledge of clinical trial design, regulatory compliance, and data analysis, typically supported by a medical, pharmaceutical, or life sciences degree along with significant experience in clinical research. Expertise in systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and familiarity with GCP, FDA, and ICH guidelines are essential, and certifications like CCRP or CCRA are highly valued. Leadership, strategic thinking, and strong communication skills distinguish top performers by enabling effective team management and stakeholder engagement. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with all regulatory standards, driving successful research outcomes.

What are some of the main challenges a clinical research director faces when overseeing multiple clinical trials simultaneously?

One of the primary challenges for a Clinical Research Director managing multiple trials is ensuring consistent protocol adherence across diverse study sites while maintaining strict regulatory compliance. Balancing resource allocation, addressing unforeseen issues such as patient recruitment delays, and effectively communicating with cross-functional teams also require strong organizational and leadership skills. Additionally, the director must stay updated on evolving industry standards and regulatory requirements to mitigate risks and ensure the integrity of all ongoing studies.

What is the difference between Clinical Research Director vs Clinical Research Manager?

AspectClinical Research DirectorClinical Research Manager
ResponsibilitiesOversees multiple projects, strategic planning, and department leadershipManages daily operations of clinical trials, supervises teams, and ensures compliance
Required CredentialsTypically requires a PhD, MD, or advanced degree, along with extensive experienceUsually requires a bachelor's or master's degree in life sciences, with relevant experience
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, overseeing multiple teamsOperational setting within research sites or CROs, directly managing trial teams
Industry UsageCommonly found in large organizations with multiple projectsFound in both large and small organizations, focusing on trial execution

The Clinical Research Director focuses on strategic oversight and leadership of research programs, while the Clinical Research Manager handles day-to-day trial management. Both roles require relevant experience, but the director's role is more senior and strategic.

More about Clinical Research Director jobs

What are the most commonly searched types of Clinical Research jobs in Riverside, RI?

The most popular types of Clinical Research jobs in Riverside, RI are:

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The top searched job categories for Clinical Research Director jobs in Riverside, RI are:

What cities near Riverside, RI are hiring for Clinical Research Director jobs?

Cities near Riverside, RI with the most Clinical Research Director job openings:

Clinical Research Director jobs near you
Infographic showing various Clinical Research Director job openings in Riverside, RI as of June 2026, with employment types broken down into 3% As Needed, 89% Full Time, 7% Part Time, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $110,918 per year, or $53.3 per hour.

Senior Associate, Clinical Outcome Assessment (Real World Research)

Parexel

Carolina, RI • On-site, Remote

Full-time

Posted 25 days ago

Key responsibilities

  • Complete assigned activities within project scope and objectives, ensuring timely delivery and quality standards.

  • Identify and communicate project and internal issues to senior colleagues and propose solutions.

  • Produce quality work within broad project guidelines, prioritizing tasks to achieve project outcomes.

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

34th of 75 rated research

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Purpose of this Role;

A Senior Associate, under the general direction of a Project Lead and Technical SMEs,takes responsibility for ensuring that client work is performed, and delivered on time, meeting the qualityexpectations of Parexel Consulting and the client.

Essential experience, skills & educational you will be required to have to be considered for this role;

Knowledge and Experience:
*Ideally 2-3 years' relevant clinical experience in an industry-related or consulting environment conducting qualitative interview studies.

*Proficiency using software for the analysis of qualitative interview data (e.g. Atlas.TI).

*Experience with Clinical Outcomes Assessment (COA) development and validation best practice is preferred.

Skills:
Client-Centric and Quality Excellence
Results-Driven
Interpersonal Effectiveness and Communication
Team Effectiveness and Collaborative
Business Solutions & Problem-Solving
English language proficiency and communication excellence

Proficiency in other languages desirable

Education:
Minimum of a Bachelor's Degree in a Scientific or Technical Discipline.
Ideally a Postgraduate degree in a Clinical Outcomes Assessment Scientific or Technical Discipline (Psychology, Social Science,Anthropology)

Key Responsibilities of this role include;

-Consulting Activities and Relationship Management

Completes assigned activities within project scope and objectives with
an understanding of issues which may impact project profitability under
the direction of the project lead/ manager
Identifies project and internal issues to senior colleagues and project
lead/ manager and provides proposed solutions

Identifies and alerts Parexel Consulting management to opportunities for follow-onbusiness or necessary changes in project scope

Follows and implements the organization's consulting models and methodologies under the guidance of the Project Lead and/or Technical SMEs

Delivers consulting services within personal area of expertise under the guidance of the Project Lead and Technical SME

May assist in preparing and/ or delivering a presentation with the support of senior colleagues

-Project Execution

Works effectively within a team environment but may work independently delivering services within their area of competence

Works within broad project guidelines as directed by the project lead/ manager and/or Technical SMEs

Produces quality work that meets the expectations of project lead/ manager and the client

Takes initiative to prioritize work to achieve specified project outcomes while confirming alignment with project lead and line manager

Applies information provided by the project lead/manager or senior colleagues to complete assigned project activities

-Business Development

Continue to build a network of industry colleagues through relationships formed during project engagements or through other industry experience

What Parexel employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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