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Clinical Study Manager Jobs in Oregon (NOW HIRING)

BIOTRONIK SE & Co.KG

$100 - $125/hr

Provide day-to-day study management and support to investigative sites. * Serve as a clinical and technical resource for site coordinators, investigators, field clinical personnel, sales ...

Natera

Senior Manager, Clinical Trials

OR · On-site +1

Manage study contracting, budget and payment process for all clinical trial vendors including investigational sites. * Partner with department head to develop department procedures and develop ...

Oregonstate

Study Abroad Manager

Corvallis, OR · On-site

Position Summary This Study Abroad Manager position takes the lead role with the development and execution of a suite of 30+ OSU faculty-led programs across the university, and oversees the OSU GO ...

Avalyn Pharma

Director, Clinical Development

OR · On-site +1

... Management, and external CROs to support effective trial execution and alignment with overall ... Study Design & Strategy * Lead clinical trial strategy and protocol development, including ...

Telix Pharmaceuticals (AMER)

Global Clinical Lead

OR · On-site +1

Clinical study design and execution : Oversee the development of clinical study plans from concept ... Leadership and project management : Demonstrated success in leading cross-functional teams and ...

Syneoshealth

Clinical Trial Manager - Full Service

OR · On-site +1

Reviews the study scope of work, budget and protocol content and ensures the clinical project team ... Data Management Plan, Communication Plan) as they relate to the clinical trial management ...

Natera

Manager, Clinical Trials

OR · On-site +1

Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites * Lead study-related activities such as protocol and ...

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Clinical Study Manager information

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$30

$66

$101

How much do clinical study manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical study manager in Oregon is $66.10, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $74.47 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

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.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

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 timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are the most commonly searched types of Clinical Study jobs in Oregon?

The most popular types of Clinical Study jobs in Oregon are:

What are popular job titles related to Clinical Study Manager jobs in Oregon?

For Clinical Study Manager jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Oregon look for?

The top searched job categories for Clinical Study Manager jobs in Oregon are:

What cities in Oregon are hiring for Clinical Study Manager jobs?

Cities in Oregon with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Oregon as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $137,483 per year, or $66.1 per hour.

Clinical Studies Engineer II

Biotronik

Lake Oswego, OR • On-site

Full-time

Posted 14 days ago

Key responsibilities

  • Participate in all phases of clinical investigations, including study design, initiation, enrollment, study execution, data analysis, and clinical report writing.

  • Lead the development and revision of clinical study protocols and design case report forms to support data collection and analysis.

  • Provide day-to-day study management and support to investigative sites, including training, monitoring, and resolving data discrepancies.

Job description

Clinical Studies Engineer II
BIOTRONIK is one of the leading manufacturers of cardio- and endovascular implants and catheters for cardiac rhythm management, electrophysiology and vascular intervention. As a globally active company headquartered in Berlin, Germany, we develop, produce and distribute high-quality medical products based on the latest technology and research. Our success is based on the competence and results-oriented cooperation of our employees.
BIOTRONIK is seeking a Clinical Studies Engineer II to join our Clinical Studies team. In this role, you will play an important part in the planning, execution, and successful completion of clinical investigations involving innovative medical device technologies. You will develop an in-depth understanding of BIOTRONIK products, clinical procedures, and relevant therapeutic areas while serving as a clinical and technical resource for investigative sites, field personnel, and internal stakeholders. Working collaboratively with cross-functional teams, investigators, and study sites, you will support clinical investigations throughout the study lifecycle, including protocol development, study initiation, enrollment, data analysis, clinical reporting, and regulatory submissions. This role offers the opportunity to contribute to the development of clinical evidence supporting BIOTRONIK technologies while helping ensure the successful and compliant conduct of clinical studies.
Your Responsibilities
Clinical Study Management & Execution
  • Participate in all phases of clinical investigations, including study design, initiation, enrollment, study execution, data analysis, and clinical report writing.
  • Lead the development and revision of clinical study protocols.
  • Design case report forms (CRFs) to support accurate, comprehensive data collection and analysis in accordance with study protocols.
  • Develop study documents, training materials, and other resources supporting clinical protocols, study procedures, and CRF completion.
  • Provide day-to-day study management and support to investigative sites.
  • Serve as a clinical and technical resource for site coordinators, investigators, field clinical personnel, sales representatives, and other internal stakeholders.
  • Train investigative sites and BIOTRONIK personnel on clinical protocols, investigational devices, study procedures, and data collection requirements.
  • Support sites and field personnel in collecting complete, accurate, timely, and compliant clinical data.
  • Review and/or monitor case report forms, source documents, and other study records in accordance with BIOTRONIK procedures and applicable regulatory requirements.
  • Collaborate with study teams, field personnel, and investigative sites to resolve data discrepancies, compliance concerns, and regulatory issues.
  • Identify and report significant protocol compliance issues and support appropriate resolution.
  • Develop solutions to logistical and operational challenges that arise during study execution and communicate recommendations to appropriate stakeholders.
  • Build and maintain strong professional relationships with investigators and investigative sites.

Data Analysis, Reporting & Regulatory Support
  • Partner with Clinical Data Operations to clean, organize, summarize, and analyze complex clinical data.
  • Generate clinical reports and contribute to scientific publications.
  • Support preparation of clinical content for FDA submissions.
  • Participate in FDA meetings as a clinical representative when needed, including presenting and explaining device features, clinical study design, and study results.

Product & Technical Expertise
  • Develop an in-depth understanding of BIOTRONIK products and associated clinical procedures, which may include technologies within cardiac rhythm management, vascular intervention, and/or spinal cord stimulation.
  • Develop training and clinical study support materials for investigational or study devices and procedures.
  • Collaborate with Advanced Product Support and other internal teams to address technical and study-related questions.
  • Attend device implants and/or follow-up procedures as needed to remain current on devices, clinical utilization, and patient care.
  • Provide clinical and technical feedback to Engineering and Research & Development teams as needed.
  • Contribute clinical expertise to new project planning and development initiatives.
  • Support the training and mentoring of newly hired Clinical Studies Engineers.
  • Provide support to other clinical studies and projects as business needs require.

What We're Looking For
Required Qualifications
  • Bachelor's degree in a health profession, science, engineering, or related field with a strong technical and clinical background.
  • Working knowledge of FDA regulations, ICH guidelines, Good Clinical Practice (GCP), and other regulations and standards governing clinical research.
  • Demonstrated ability to develop expertise in relevant therapeutic areas and quickly learn and integrate knowledge of new technologies and clinical applications.
  • Strong written and verbal communication, presentation, and interpersonal skills.
  • Excellent organizational skills and attention to detail.
  • Ability to manage multiple priorities and work effectively both independently and as part of a cross-functional team.
  • Strong computer skills and ability to work effectively with clinical study data and documentation.

Clinical Studies Experience
Candidates must meet one of the following:
  • More than three years of successful experience as a Clinical Studies Engineer I within BIOTRONIK's Clinical Studies department, along with completion of Clinical Studies Certification in a product area of primary study support; or
  • Comparable clinical studies experience with another organization in a similar position or relevant field.

Preferred Qualifications
  • Master's degree in a health profession, science, engineering, or related discipline.
  • Experience in a clinical setting, biostatistics, IDE clinical studies, and/or medical device support.
  • Previous experience supporting medical device clinical investigations.

Work Location
Work location is hybrid out of our Lake Oswego, Oregon campus -or- remote within the United States based on skill set and qualifications.
Travel Requirements
  • Travel is generally limited to less than two weeks per year for clinical procedures, investigative site training, and meetings. Depending on study needs and the phase of a clinical investigation, travel may periodically increase to up to 25%.

Physical Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to be independently mobile.
  • The employee is also required to interact with a computer for extended periods of time, and communicate with co-workers.
  • Must be able to work a minimum of 40 hours / week.
  • Must be able to travel

Are you interested? Please apply online through our application management system! We are looking forward to welcoming you.
Location: Lake Oswego, OR | Working hours: Full-time | Type of contract: Undefined
Apply now under: www.biotronik.com/careers
Job ID: 62605 | USA | BIOTRONIK Inc.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law. Please note that applications sent by post will only be returned if a sufficiently stamped self-addressed envelope is included.

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