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Clinical Study Manager Jobs in Remote, OR (NOW HIRING)

TechData Service Company LLC

Medical Writer (Remote)

OR · Remote

$85 - $90/hr

Collaborate with cross-functional teams to manage document timelines, review cycles, and submission ... Knowledge of drug development, clinical research, clinical study conduct, regulatory requirements ...

Nexpro Technologies Inc

Be Seen First

Senior Clinical Research Associate

OR · Remote

$90K - $120K/yr

Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, SOPs, and ... Support study start-up, patient recruitment, and site management activities. * Ensure studies are ...

Nexpro Technologies Inc

Be Seen First

Senior Clinical Research Associate

OR · Remote

$90K - $120K/yr

Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, SOPs, and ... Support study start-up, patient recruitment, and site management activities. * Ensure studies are ...

Reliant Rehabilitation

Physical Therapist

Myrtle Point, OR · On-site

$1.5K - $2.0K/wk

... management. The therapist upholds professional conduct and complies with all state and federal ... clinical and leadership skills through collaboration, self-study, and continuing education Maintain ...

Reliant Rehabilitation

Physical Therapist

Myrtle Point, OR · On-site

$45 - $60/hr

... management. The therapist upholds professional conduct and complies with all state and federal ... clinical and leadership skills through collaboration, self-study, and continuing education • ...

Reliant Rehabilitation

Physical Therapist

Myrtle Point, OR

$1.5K - $2.0K/wk

... management. The therapist upholds professional conduct and complies with all state and federal ... clinical and leadership skills through collaboration, self-study, and continuing education Maintain ...

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All JobsClinical Study JobsClinical Study Manager JobsClinical Study Manager Jobs in Remote, OR

Clinical Study Manager information

See Remote, OR salary details

$28

$62

$96

How much do clinical study manager jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical study manager in Remote, OR is $62.45, according to ZipRecruiter salary data. Most workers in this role earn between $50.67 and $70.38 per hour, depending on experience, location, and employer.

Is CRC an entry level position?

A Clinical Research Coordinator (CRC) is often considered an entry-level role in clinical research, requiring basic knowledge of study protocols and good clinical practice (GCP). However, some positions may prefer prior healthcare or research experience, and advancement typically involves gaining additional certifications or experience. The role often serves as a stepping stone to more senior positions like Clinical Study Manager.

What are the key skills and qualifications needed to thrive as a Clinical Study Manager, and why are they important?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by Clinical Study Managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, such as coordinating trials or working in related roles. Entry-level roles in clinical research often include Clinical Trial Assistant or Clinical Research Coordinator, while CRAs often need knowledge of Good Clinical Practice (GCP) and relevant certifications like CCRP or RAC.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage budgets, and ensure data quality, often using specialized software and requiring strong organizational skills. Their role is essential for the successful completion of clinical research projects.

How much does a clinical trials manager make?

A clinical study manager typically earns between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and responsibilities.
What are popular job titles related to Clinical Study Manager jobs in Remote, OR? For Clinical Study Manager jobs in Remote, OR, the most frequently searched job titles are:
What job categories do people searching Clinical Study Manager jobs in Remote, OR look for? The top searched job categories for Clinical Study Manager jobs in Remote, OR are:
What cities near Remote, OR are hiring for Clinical Study Manager jobs? Cities near Remote, OR with the most Clinical Study Manager job openings:
Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Remote, OR as of July 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $129,906 per year, or $62.5 per hour.
Medical Writer (Remote)

Medical Writer (Remote)

TechData Service Company LLC

OR • Remote

$85 - $90/hr

Contractor

Medical, Dental

This job post has expired today. Applications are no longer accepted.

Job description

Company: Biotechnology Company

Title: Medical Writer

Contract Position - 6 months with potential extension

Position Summary
Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in support of clinical development and regulatory submissions. This role will partner with Clinical Development, Regulatory Affairs, Biostatistics, Medical Affairs, Quality Assurance, and external vendors to produce clear, accurate, and compliant documents.
Key Responsibilities
Author, review, and edit clinical and regulatory documents, including protocols, protocol amendments, clinical study reports, investigator’s brochures, informed consent forms, CTD clinical modules, briefing documents, safety reports, and responses to regulatory questions.
Support clinical development activities by helping prepare clinical development plans, protocols, and related study documents.
Interpret complex clinical and scientific data and communicate findings clearly and accurately.
Ensure documents comply with ICH, GCP, FDA, EMA, and other applicable regulatory guidelines.
Collaborate with cross-functional teams to manage document timelines, review cycles, and submission-ready deliverables.
Review documents prepared by internal teams or external vendors for clarity, consistency, scientific accuracy, and regulatory compliance.
Qualifications
Advanced degree preferred, such as PhD, PharmD, MD, or MSc in Life Sciences, Medicine, Pharmacy, or a related field.
Minimum 3–5 years of medical writing experience in the pharmaceutical, biotech, or CRO industry.
Strong experience writing clinical trial and regulatory submission documents.
Knowledge of drug development, clinical research, clinical study conduct, regulatory requirements, and biostatistical concepts.
Familiarity with medical terminology and coding dictionaries such as MedDRA and WHODrug.
Strong knowledge of ICH/GCP and regulatory submission requirements.
Epilepsy or neurology experience is a plus.
Veeva experience preferred.
Proficiency with Microsoft Word, Excel, PowerPoint, Adobe Acrobat, EndNote, and document management systems.
Ideal Candidate
The ideal candidate is a detail-oriented medical writer who can manage multiple projects, work independently, collaborate effectively with cross-functional teams, and produce clear, well-structured, submission-ready clinical and regulatory documents.

Company Description

www.techdataservice.com