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 ...
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 ...
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 ...
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 ...
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 ...
Description The Study Project Lead will lead client support of the Randomization and Trial Supply Management (RTSM) application after clinical study go-live. The Support Project Lead is responsible ...
New
Description The Study Project Lead will lead client support of the Randomization and Trial Supply Management (RTSM) application after clinical study go-live. The Support Project Lead is responsible ...
New
The Study Project Lead will lead client support of the Randomization and Trial Supply Management (RTSM) application after clinical study go-live. The Support Project Lead is responsible for the ...
The Study Project Lead will lead client support of the Randomization and Trial Supply Management (RTSM) application after clinical study go-live. The Support Project Lead is responsible for the ...
OR · On-site +1
The SCPM ensures completion of study deliverables and proactively identifies and resolves clinical project issues. Key Accountabilities * Proactively managing all aspects of the trial process ...
OR · On-site +1
The SCPM ensures completion of study deliverables and proactively identifies and resolves clinical project issues. Key Accountabilities * Proactively managing all aspects of the trial process ...
OR · On-site +1
Medical
Dental
Vision
Retirement
PTO
Manage study timelines, deliverables, risks, and issue resolution * Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers * Coordinate Clinical Trial Team ...
OR · On-site +1
Medical
Dental
Vision
Retirement
PTO
Manage study timelines, deliverables, risks, and issue resolution * Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers * Coordinate Clinical Trial Team ...
S/he is responsible for completion of all study deliverables, ensuring the highest level of data ... Proficient in clinical trial management systems including electronic data capture (EDC) software ...
S/he is responsible for completion of all study deliverables, ensuring the highest level of data ... Proficient in clinical trial management systems including electronic data capture (EDC) software ...
OR · On-site +1
Manage study activities in the successful execution of clinical trials from protocol concept to clinical study report, complying with Good Clinical Practice (GCP) guidelines and international ...
OR · On-site +1
Manage study activities in the successful execution of clinical trials from protocol concept to clinical study report, complying with Good Clinical Practice (GCP) guidelines and international ...
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 ...
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 ...
OR · On-site +1
$79K - $108K/yr
Flexibility to engage with clinical collaborators and study teams across international, global time zones * Ability to engage in work-related international and domestic travel up to 25% to manage ...
OR · On-site +1
$79K - $108K/yr
Flexibility to engage with clinical collaborators and study teams across international, global time zones * Ability to engage in work-related international and domestic travel up to 25% to manage ...
OR · On-site +1
Develop study-related documents with minimal Clinical Trial Manager guidance including: protocol, informed consent forms, training materials, protocol amendments, monitoring plans, synopses, and ...
OR · On-site +1
Develop study-related documents with minimal Clinical Trial Manager guidance including: protocol, informed consent forms, training materials, protocol amendments, monitoring plans, synopses, and ...
OR · On-site
... managing the clinical scientists embedded within the biobanking workstream. PRIMARY RESPONSIBILITIES: Trial Strategy and Protocol Architecture * Design robust clinical study concepts, specifying ...
OR · On-site +1
Medical
Dental
Vision
Retirement
PTO
The Central Study Coordinator (CSC) position combines clinical research and project management skillsinto a singular role that delivers a strong customer experience for both patients and sites. Often ...
OR · On-site +1
Medical
Dental
Vision
Retirement
PTO
The Central Study Coordinator (CSC) position combines clinical research and project management skillsinto a singular role that delivers a strong customer experience for both patients and sites. Often ...
OR · On-site +1
Medical
Dental
Vision
Retirement
PTO
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated ... You will oversee timelines, budgets, operational risks, study start-up activities, vendor ...
OR · On-site +1
Medical
Dental
Vision
Retirement
PTO
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated ... You will oversee timelines, budgets, operational risks, study start-up activities, vendor ...
OR · On-site +1
$215K - $230K/yr
Medical
Retirement
PTO
Lead/Contribute to study design and amendments in collaboration with internal and external ... Collaborate with clinical operations, data management and CRO to develop and implement the overall ...
OR · On-site +1
$215K - $230K/yr
Medical
Retirement
PTO
Lead/Contribute to study design and amendments in collaboration with internal and external ... Collaborate with clinical operations, data management and CRO to develop and implement the overall ...
OR · On-site +1
Medical
Dental
Vision
Retirement
PTO
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 ...
OR · On-site +1
Medical
Dental
Vision
Retirement
PTO
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 ...
About the Role The Sr. Clinical Research Associate (Sr. CRA) is responsible for managing and ... studies. * Demonstrates ability to coordinate, organize, communicate, and manage site activities ...
About the Role The Sr. Clinical Research Associate (Sr. CRA) is responsible for managing and ... studies. * Demonstrates ability to coordinate, organize, communicate, and manage site activities ...
Portland, OR · On-site
$60K - $91K/yr
Required Qualifications: * 3 or more years Clinical research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance
Portland, OR · On-site
$60K - $91K/yr
Required Qualifications: * 3 or more years Clinical research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance
Portland, OR · On-site
$60K - $91K/yr
Required Qualifications: * 3 or more years Clinical research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance
Portland, OR · On-site
$60K - $91K/yr
Required Qualifications: * 3 or more years Clinical research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance
Salem, OR · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Salem, OR · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
$30.50 - $36.97
4% of jobs
$36.97 - $43.44
6% of jobs
$43.44 - $49.91
7% of jobs
$54.76 is the 25th percentile. Wages below this are outliers.
$49.91 - $56.38
9% of jobs
$56.38 - $62.85
15% of jobs
The median wage is $65.70 / hr.
$62.85 - $69.31
18% of jobs
$73.92 is the 75th percentile. Wages above this are outliers.
$69.31 - $75.78
21% of jobs
$75.78 - $82.25
7% of jobs
$82.25 - $88.72
6% of jobs
$88.72 - $95.19
3% of jobs
$95.19 - $101.66
2% of jobs
$30
$66
$101
The most popular types of Clinical Study jobs in Oregon are:
For Clinical Study Manager jobs in Oregon, the most frequently searched job titles are:
The top searched job categories for Clinical Study Manager jobs in Oregon are:
Cities in Oregon with the most Clinical Study Manager job openings:

7.7
Based on 38 frontline employees who took The Breakroom Quiz
56th of 120 rated laboratories
POSITION SUMMARY:
This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to support the development, validation, and commercialization non-invasive molecular diagnostic tests. This role manages clinical operations staff and all aspects of the trials independently, including study design, protocol implementation, site monitoring, and recruitment site management.
PRIMARY RESPONSIBILITIES:
Responsible for the implementation of clinical trial activities per study protocol. Works closely with investigative site personnel, CROs, and other study vendors
Manage and coach clinical research staff.
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 infrastructure.
Design study related documents, including but not limited to study protocol, informed consent forms, CRFs, and regulatory binders.
Train CROs, vendors, investigators and study coordinators on study protocol and relevant
Monitor and track clinical trial progress and provide status update to stakeholders.
Partner with other research and development groups to achieve deliverables.
This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job
Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire.
Must maintain a current status on Natera training requirements.
QUALIFICATIONS:
Bachelor's degree in life sciences, other relevant discipline, or equivalent required. Advanced degree preferred.
5-10 years of clinical research experience, including at least 3-5 years of experience in managing clinical trials as a leading role.
2+ years of experience of managing staff. Experience in managing CROs is preferred.
Experience managing all aspects of the trials independently, including study design, protocol implementation, site monitoring, sample management, and recruitment site management.
KNOWLEDGE, SKILLS, AND ABILITIES:
Familiar with the clinical research regulations.
Ability to collaborate with the study team, cross functional team members and external
Proficiency in MS Word, Excel and PowerPoint.
Good organization and planning skills.
Strong interpersonal skills and communication skills (both written and oral).
Strong leadership skills, self-motivated, adaptable to a dynamic and fast paced environment.