Clinical Trial Manager
Bellevue, WAFull-time
90K–120K a year
Behavioral Health Market Context
Apply Nowvia Jooble
Benefits
$90,000 – $120,000 DOE | Sign-On BonusSalary: $90,000 – $120,000, commensurate with experience and qualificationsSign-on bonusFull-time position with competitive benefitsWe also welcome applications from U.S.-trained and internationally trained medical graduatesPay: $90,000.00 - $120,000.00 per year401(k)Dental insuranceHealth insurancePaid time offVision insurance
Job Description
CLINICAL TRIAL MANAGER
Bellevue, Washington | Full-Time | On-Site
$90,000 – $120,000 DOE | Sign-On Bonus
IMPORTANT REQUIREMENT — PLEASE READ BEFORE APPLYING:
This role requires an MD, DO, or an international equivalent medical degree. Applications without this qualification will not move forward.
ABOUT US
We are a physician-led clinical research program specializing in rheumatology and autoimmune diseases, supported by a well-established specialty practice with over 30 years of excellence in patient care.
Our team conducts Phase 2–4 industry-sponsored trials in conditions such as Sjögren’s syndrome, gout, and systemic autoimmune diseases. With strong patient access and a growing research portfolio, we are advancing innovative therapies that improve outcomes for patients with complex rheumatologic conditions.
THE OPPORTUNITY
As Clinical Trial Manager, you will serve as the primary operational and strategic leader for all active and incoming clinical trials. You will work closely with the Principal Investigator, sponsor representatives, regulatory bodies, and a dedicated clinical team to ensure the highest standards of trial conduct, data integrity, and patient safety.
REQUIREMENTS
• MD, DO, or international equivalent medical degree (required)
• Minimum 2 years of clinical trial management experience (required)
• Strong working knowledge of FDA regulations, ICH-GCP guidelines, and IRB processes
• Proficiency with EDC systems, CTMS platforms, and essential document management
WHO YOU ARE
• A strategic thinker who anticipates risks and develops proactive solutions
• A self-starter who takes ownership without being told what needs to be done
• Energetic and enthusiastic with an unwavering commitment to excellence
• An exceptional communicator — written, verbal, and cross-functional
• Experienced collaborating with sponsors, CROs, IRBs, vendors, and internal teams
• Deeply knowledgeable about Good Clinical Practice (GCP) and research ethics
• Comfortable in a fast-moving, growth-oriented environment
• Possess a genuine growth mindset — you seek feedback, embrace challenges, continuously improve, and inspire the same in those around you
RESPONSIBILITIES
• Develop and manage the overall strategy, timeline, and execution of all active clinical trials
• Serve as the primary point of contact for sponsors, CROs, and regulatory bodies
• Oversee site-wide implementation and compliance with GCP standards
• Monitor and manage clinical trial team activities and protocol adherence
• Ensure all regulatory and ethical requirements — including IRB submissions and renewals — are met on time
• Collaborate with clinical, billing, pharmacy, and administrative teams to drive trial success
• Monitor and report trial progress to the PI and sponsor; escalate issues promptly
• Anticipate and mitigate operational, regulatory, and safety risks
• Build and maintain strong relationships with vendors, sites, and sponsors
• Ensure all trial documentation and the Investigator Site File (ISF) are complete and audit-ready at all times
• Develop, manage, and monitor clinical trial budgets; negotiate site payments, track expenditures, and ensure financial accountability across all active studies
COMPENSATION & BENEFITS
• Salary: $90,000 – $120,000, commensurate with experience and qualifications
• Sign-on bonus
• Full-time position with competitive benefits
• We also welcome applications from U.S.-trained and internationally trained medical graduates.
Pay: $90,000.00 - $120,000.00 per year
Benefits:
• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance
Application Question(s):
• Do you have extensive experience as a Clinical Investigator in industry-sponsored clinical trials?
• Do you have strong knowledge of FDA regulations, ICH-GCP, and clinical research compliance?
• Do you have proven leadership experience in clinical research operations?
• Do you have experience with regulatory systems, audit management, and inspection readiness?
• Prior experience in financial oversight of clinical trials (budgets/contracts)?
• Did you read the entire job description and do you understand that this role is only open to candidates who currently reside in the Seattle/Greater Puget Sound area or Washington State?
Education:
• Doctorate (Required)
Experience:
• Scaling a clinical research program: 4 years (Preferred)
• Successful study enrollment & sponsor engagement: 4 years (Preferred)
License/Certification:
• MD/DO or International equivalent (Required)
• Teaching/research medical license in Washington State (Required)
Location:
• Bellevue, WA 98007 (Required)
Work Location: In person
Bellevue, Washington | Full-Time | On-Site
$90,000 – $120,000 DOE | Sign-On Bonus
IMPORTANT REQUIREMENT — PLEASE READ BEFORE APPLYING:
This role requires an MD, DO, or an international equivalent medical degree. Applications without this qualification will not move forward.
ABOUT US
We are a physician-led clinical research program specializing in rheumatology and autoimmune diseases, supported by a well-established specialty practice with over 30 years of excellence in patient care.
Our team conducts Phase 2–4 industry-sponsored trials in conditions such as Sjögren’s syndrome, gout, and systemic autoimmune diseases. With strong patient access and a growing research portfolio, we are advancing innovative therapies that improve outcomes for patients with complex rheumatologic conditions.
THE OPPORTUNITY
As Clinical Trial Manager, you will serve as the primary operational and strategic leader for all active and incoming clinical trials. You will work closely with the Principal Investigator, sponsor representatives, regulatory bodies, and a dedicated clinical team to ensure the highest standards of trial conduct, data integrity, and patient safety.
REQUIREMENTS
• MD, DO, or international equivalent medical degree (required)
• Minimum 2 years of clinical trial management experience (required)
• Strong working knowledge of FDA regulations, ICH-GCP guidelines, and IRB processes
• Proficiency with EDC systems, CTMS platforms, and essential document management
WHO YOU ARE
• A strategic thinker who anticipates risks and develops proactive solutions
• A self-starter who takes ownership without being told what needs to be done
• Energetic and enthusiastic with an unwavering commitment to excellence
• An exceptional communicator — written, verbal, and cross-functional
• Experienced collaborating with sponsors, CROs, IRBs, vendors, and internal teams
• Deeply knowledgeable about Good Clinical Practice (GCP) and research ethics
• Comfortable in a fast-moving, growth-oriented environment
• Possess a genuine growth mindset — you seek feedback, embrace challenges, continuously improve, and inspire the same in those around you
RESPONSIBILITIES
• Develop and manage the overall strategy, timeline, and execution of all active clinical trials
• Serve as the primary point of contact for sponsors, CROs, and regulatory bodies
• Oversee site-wide implementation and compliance with GCP standards
• Monitor and manage clinical trial team activities and protocol adherence
• Ensure all regulatory and ethical requirements — including IRB submissions and renewals — are met on time
• Collaborate with clinical, billing, pharmacy, and administrative teams to drive trial success
• Monitor and report trial progress to the PI and sponsor; escalate issues promptly
• Anticipate and mitigate operational, regulatory, and safety risks
• Build and maintain strong relationships with vendors, sites, and sponsors
• Ensure all trial documentation and the Investigator Site File (ISF) are complete and audit-ready at all times
• Develop, manage, and monitor clinical trial budgets; negotiate site payments, track expenditures, and ensure financial accountability across all active studies
COMPENSATION & BENEFITS
• Salary: $90,000 – $120,000, commensurate with experience and qualifications
• Sign-on bonus
• Full-time position with competitive benefits
• We also welcome applications from U.S.-trained and internationally trained medical graduates.
Pay: $90,000.00 - $120,000.00 per year
Benefits:
• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance
Application Question(s):
• Do you have extensive experience as a Clinical Investigator in industry-sponsored clinical trials?
• Do you have strong knowledge of FDA regulations, ICH-GCP, and clinical research compliance?
• Do you have proven leadership experience in clinical research operations?
• Do you have experience with regulatory systems, audit management, and inspection readiness?
• Prior experience in financial oversight of clinical trials (budgets/contracts)?
• Did you read the entire job description and do you understand that this role is only open to candidates who currently reside in the Seattle/Greater Puget Sound area or Washington State?
Education:
• Doctorate (Required)
Experience:
• Scaling a clinical research program: 4 years (Preferred)
• Successful study enrollment & sponsor engagement: 4 years (Preferred)
License/Certification:
• MD/DO or International equivalent (Required)
• Teaching/research medical license in Washington State (Required)
Location:
• Bellevue, WA 98007 (Required)
Work Location: In person
Qualifications
- •This role requires an MD, DO, or an international equivalent medical degree
- •MD, DO, or international equivalent medical degree (required)
- •Minimum 2 years of clinical trial management experience (required)
- •Strong working knowledge of FDA regulations, ICH-GCP guidelines, and IRB processes
- •Proficiency with EDC systems, CTMS platforms, and essential document management
- •A strategic thinker who anticipates risks and develops proactive solutions
- •A self-starter who takes ownership without being told what needs to be done
- •Energetic and enthusiastic with an unwavering commitment to excellence
- •An exceptional communicator — written, verbal, and cross-functional
- •Experienced collaborating with sponsors, CROs, IRBs, vendors, and internal teams
- •Deeply knowledgeable about Good Clinical Practice (GCP) and research ethics
- •Comfortable in a fast-moving, growth-oriented environment
- •Possess a genuine growth mindset — you seek feedback, embrace challenges, continuously improve, and inspire the same in those around you
- •Do you have extensive experience as a Clinical Investigator in industry-sponsored clinical trials?
- •Do you have strong knowledge of FDA regulations, ICH-GCP, and clinical research compliance?
- •Do you have proven leadership experience in clinical research operations?
- •Do you have experience with regulatory systems, audit management, and inspection readiness?
- •Doctorate (Required)
- •MD/DO or International equivalent (Required)
- •Teaching/research medical license in Washington State (Required)
Responsibilities
- •As Clinical Trial Manager, you will serve as the primary operational and strategic leader for all active and incoming clinical trials
- •You will work closely with the Principal Investigator, sponsor representatives, regulatory bodies, and a dedicated clinical team to ensure the highest standards of trial conduct, data integrity, and patient safety
- •Develop and manage the overall strategy, timeline, and execution of all active clinical trials
- •Serve as the primary point of contact for sponsors, CROs, and regulatory bodies
- •Oversee site-wide implementation and compliance with GCP standards
- •Monitor and manage clinical trial team activities and protocol adherence
- •Ensure all regulatory and ethical requirements — including IRB submissions and renewals — are met on time
- •Collaborate with clinical, billing, pharmacy, and administrative teams to drive trial success
- •Monitor and report trial progress to the PI and sponsor; escalate issues promptly
- •Anticipate and mitigate operational, regulatory, and safety risks
- •Build and maintain strong relationships with vendors, sites, and sponsors
- •Ensure all trial documentation and the Investigator Site File (ISF) are complete and audit-ready at all times
- •Develop, manage, and monitor clinical trial budgets; negotiate site payments, track expenditures, and ensure financial accountability across all active studies
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