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Study Director Jobs in Oregon (NOW HIRING)

This highly visible role partners with Business Development, Proposal Development, Clinical Operations, and Study Teams to support growth initiatives, client engagement, therapeutic strategy, and ...

Position Summary This Study Abroad Manager position takes the lead role with the development and ... Advise faculty program directors on risk assessment, emergency planning, incident response ...

How This Role Makes a Difference Reporting to the Sr. Director of Study Feasibility & Clinical Partnerships, the Associate Director and Director of Study Feasibility & Clinical Partnerships provides ...

OR · On-site

Adapt to study specific requirements and priorities, including alternative ways of handing off patient referrals to sites (direct schedule, warm transfer, etc.) * Follow-up and interact with study ...

OR · On-site

$79K - $108K/yr

We are seeking a Director, Clinical Science to architect trial strategies and protocol execution ... Design robust clinical study concepts, specifying overall design parameters, schedules of ...

Emphasizes building self-directed learning skills and connects study skills to long-term academic success and lifelong learning. * Curriculum Awareness & Adaptive Instruction: Familiar with study ...

Director, Clinical Development

OR · On-site

$75K - $102K/yr

Position Overview The Director, Clinical Development will serve as Clinical Lead for assigned ... Design and oversee clinical studies ensuring scientific rigor, regulatory compliance, and alignment ...

Director, Clinical Development

OR · On-site +1

$75K - $102K/yr

Position Overview The Director, Clinical Development will serve as Clinical Lead for assigned ... Design and oversee clinical studies ensuring scientific rigor, regulatory compliance, and alignment ...

OR · On-site

Design robust clinical study concepts, specifying overall design parameters, sample-size logic ... Partner with Medical Directors and cross-departmental project leads to translate raw trial evidence ...

$245K - $260K/yr

At Arcus, the Director, Clinical Pharmacology (CP) functions as the Clinical Pharmacology (CP) team ... This includes design and execution of clinical pharmacology studies, design of clinical ...

Director Biostatistics

OR · Remote

$200K - $230K/yr

Director Biostatistics The Director, Biostatistics will lead the full scope of statistical strategy ... Design clinical studies, including endpoints, estimands, and sample size calculations * Serve as ...

The Director is responsible for growing the ministry by praying, staffing, and funding the area ... Follow a spiritual rhythm including daily prayer and Bible study to seek the Lord's will for the ...

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Showing results 1-20

Study Director information

See Oregon salary details

$47.6K

$135.7K

$245.8K

How much do study director jobs pay per year?

As of Aug 10, 2026, the average yearly pay for study director in Oregon is $135,721.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,300.00 and $199,300.00 per year, depending on experience, location, and employer.

What is the difference between Study Director vs Laboratory Manager?

AspectStudy DirectorLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and relevant certificationsRequires relevant degrees and management experience, but not necessarily advanced research credentials
Work EnvironmentLeads specific research or regulatory studies, often in contract labs or pharmaceutical companiesOversees daily lab operations, staff, and compliance across multiple projects
Industry UsageCommonly used in GLP, clinical, and research settingsUsed broadly in laboratory settings across industries

The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.

What is a study director?

A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.

How does a study director typically collaborate with cross-functional teams during a research project?

As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.

What does a study director do?

As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

What skills and qualifications does a successful study director have?

To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.
What are the most commonly searched types of Study jobs in Oregon? The most popular types of Study jobs in Oregon are:
What are popular job titles related to Study Director jobs in Oregon? For Study Director jobs in Oregon, the most frequently searched job titles are:
What cities in Oregon are hiring for Study Director jobs? Cities in Oregon with the most Study Director job openings:
Infographic showing various Study Director job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $135,721 per year, or $65.3 per hour.

Therapeutic Area Lead (Gastroenterology)

PSI CRO

On-site

Full-time

Re-posted 17 days ago


Job description

Company Description

We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together close to 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

The Therapeutic Area Lead is responsible for supporting the strategic development of PSI's core indications and serves as a core support function. As PSI continues to expand its Gastroenterology portfolio, we are seeking a Therapeutic Area Lead with expertise in Inflammatory Bowel Disease (IBD), particularly Ulcerative Colitis and Crohn's Disease, to serve as a scientific and strategic subject matter expert across the organization.

This highly visible role partners with Business Development, Proposal Development, Clinical Operations, and Study Teams to support growth initiatives, client engagement, therapeutic strategy, and operational excellence within the GI therapeutic area.

The successful candidate will help shape PSI's long-term GI strategy while serving as a trusted advisor to both internal stakeholders and external clients.

Responsibilities

  • Supports indication-specific strategy planning and implementation across the assigned therapeutic area
  • Attends conferences in the therapeutic area and reviews supporting literature.
  • Compiles datasets, metrics, lessons learned, and performance indices on core strategic capabilities and key studies within the given therapeutic area.
  • Supports project teams within assigned indications to advise on therapeutic strategy and study-specific mitigation strategies.
  • Supports the evaluation and selection of investigative sites.
  • Participates in Investigator Meetings and key team meetings.
  • Performs protocol analysis and escalates risks to senior management.
  • Reviews essential study documents and technical manuals.
  • Performs background research on epidemiology and other aspects of the given indication.
  • Supports client engagement and business development from a therapeutic area perspective.
  • Participates in proposal development and bid defense meeting preparations.
  • Supports PSI's KOL networks within the assigned therapeutic area.
Qualifications
  • College or university degree in Life Sciences; advanced scientific degree or clinical degree is a plus.
  • At least 6 years of experience in Gastroenterology within academia, clinical practice, laboratory, biotechnology, pharmaceutical, CRO, or clinical research environments.
  • Demonstrated experience within Inflammatory Bowel Disease, particularly Ulcerative Colitis and Crohn's Disease.
  • Strong scientific and analytical capabilities.
  • Ability to review and interpret clinical protocols and study documentation.
  • Strong written and verbal communication skills.
  • Ability to build effective relationships with internal and external stakeholders.
  • Ability to work effectively across multiple functional teams.
  • Proficiency in standard MS Office applications.
Additional Information

Join a growing therapeutic strategy function and play a key role in shaping PSI's Gastroenterology portfolio. This is a unique opportunity to combine scientific expertise, strategic thinking, and business impact while collaborating with sponsors, investigators, and cross-functional teams across the organization.