Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies ... Occasional overnight travel, up to 10%, may be required to support site engagement, audits ...
New
Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies ... Occasional overnight travel, up to 10%, may be required to support site engagement, audits ...
New
Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies ... Occasional overnight travel, up to 10%, may be required to support site engagement, audits ...
New
Quick apply
Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies ... Occasional overnight travel, up to 10%, may be required to support site engagement, audits ...
New
Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies ... Occasional overnight travel, up to 10%, may be required to support site engagement, audits ...
New
Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies ... Occasional overnight travel, up to 10%, may be required to support site engagement, audits ...
New
Clinical Study Manager
Cleveland, OH · On-site
$90K - $120K/yr
Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site ... Ability to travel overnight and out-of-state occasionally (20%) Physical Requirements/ Working ...
Clinical Study Manager
Cleveland, OH · On-site
$90K - $120K/yr
Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site ... Ability to travel overnight and out-of-state occasionally (20%) Physical Requirements/ Working ...
Clinical Study Manager
Cleveland, OH · On-site
$90K - $120K/yr
Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site ... Ability to travel overnight and out-of-state occasionally (20%) Physical Requirements/ Working ...
Clinical Study Manager
Cleveland, OH · On-site
$90K - $120K/yr
Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site ... Ability to travel overnight and out-of-state occasionally (20%) Physical Requirements/ Working ...
Ability to travel 10% of working time away from work location, may include overnight/weekend travel ... Preferred Qualifications * 10+ years of experience in medical device/IVD, biotech, life science or ...
Ability to travel 10% of working time away from work location, may include overnight/weekend travel ... Preferred Qualifications * 10+ years of experience in medical device/IVD, biotech, life science or ...
Ability to travel 10% of working time away from work location, may include overnight/weekend travel ... Preferred Qualifications * 10+ years of experience in medical device/IVD, biotech, life science or ...
Ability to travel 10% of working time away from work location, may include overnight/weekend travel ... Preferred Qualifications * 10+ years of experience in medical device/IVD, biotech, life science or ...
Prior experience in medical devices, diagnostics, or IVD industry is highly desirable. Other ... overnight travel. Work Environment * Combination of field-based customer sites activities, and ...
Prior experience in medical devices, diagnostics, or IVD industry is highly desirable. Other ... overnight travel. Work Environment * Combination of field-based customer sites activities, and ...
... out of IVD and medical device clinical trials at external clinical research sites and/or ... 70%- including overnight(s), within the US. Travel may be up to 70% during project initiation ...
... out of IVD and medical device clinical trials at external clinical research sites and/or ... 70%- including overnight(s), within the US. Travel may be up to 70% during project initiation ...
Medical Device QMS Auditor
Concord, NC · Remote
$98K - $123K/yr
Candidate must be comfortable with overnight travel of 13-15 days out of every month. Essential ... Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on ...
Medical Device QMS Auditor
Concord, NC · Remote
$98K - $123K/yr
Candidate must be comfortable with overnight travel of 13-15 days out of every month. Essential ... Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on ...
Medical Device QMS Auditor
Reston, VA · On-site
$98K - $123K/yr
Candidate must be comfortable with overnight travel of 13-15 days out of every month. Essential ... Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on ...
Medical Device QMS Auditor
Reston, VA · On-site
$98K - $123K/yr
Candidate must be comfortable with overnight travel of 13-15 days out of every month. Essential ... Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on ...
Medical Device QMS Auditor
Concord, NC · Remote
$98K - $123K/yr
Candidate must be comfortable with overnight travel of 13-15 days out of every month. Essential ... Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on ...
Medical Device QMS Auditor
Concord, NC · Remote
$98K - $123K/yr
Candidate must be comfortable with overnight travel of 13-15 days out of every month. Essential ... Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on ...
... out of IVD and medical device clinical trials at external clinical research sites and/or ... Ability to travel 20-70%- including overnight(s), within the US. Travel may be up to 70% during ...
... out of IVD and medical device clinical trials at external clinical research sites and/or ... Ability to travel 20-70%- including overnight(s), within the US. Travel may be up to 70% during ...
Facility Technician III
Lodi, CA · On-site +1
$63K - $89K/yr
This includes all manufacturing areas (Plastics & IVD factories, as well as office, R+D and ... Ability to travel - 5% travel, overnight, within Lodi, SV or any other site as needed * Must have a ...
Facility Technician III
Lodi, CA · On-site +1
$63K - $89K/yr
This includes all manufacturing areas (Plastics & IVD factories, as well as office, R+D and ... Ability to travel - 5% travel, overnight, within Lodi, SV or any other site as needed * Must have a ...
... out of IVD and medical device clinical trials at external clinical research sites and/or ... Ability to travel 20-70%- including overnight(s), within the US. Travel may be up to 70% during ...
... out of IVD and medical device clinical trials at external clinical research sites and/or ... Ability to travel 20-70%- including overnight(s), within the US. Travel may be up to 70% during ...
... out of IVD and medical device clinical trials at external clinical research sites and/or ... Ability to travel 20-70%- including overnight(s), within the US. Travel may be up to 70% during ...
... out of IVD and medical device clinical trials at external clinical research sites and/or ... Ability to travel 20-70%- including overnight(s), within the US. Travel may be up to 70% during ...
Overnight Ivd information
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Full-time
Medical, Retirement, PTO
Posted 7 days ago
New
Job description
Learn more at
Castle Biosciences Inc. is growing, and we are looking to hire a full-time Clinical Research, Clinical Safety Manager working from our Phoenix, AZ, Friendswood, TX or Pittsburgh, PA office location, with a start date of August 1, 2026.
Why Castle Biosciences?
Exceptional Benefits Package:
A DAY IN THE LIFE OF AN Clinical Safety Manager
The Clinical Research Safety Manager is responsible for establishing, implementing, and continuously improving clinical research safety processes for a laboratory-developed test (LDT) and medical device organization while ensuring compliance with applicable regulations, Company policies, and Standard Operating Procedures (SOPs). This role serves as the operational safety lead for company-sponsored clinical studies, overseeing safety planning, adverse event management, risk assessments, safety reporting, and regulatory documentation for FDA-regulated LDT, IVD, and medical device studies. The position partners with cross-functional teams to ensure participant safety, regulatory compliance, inspection readiness, and alignment between clinical safety activities, quality systems, and post-market processes. This individual contributor role also supports the development of safety processes, study documentation, and training while providing support as directed by leadership and contributing to the growth of the clinical research safety function.
REQUIRED QUALIFICATIONS
*Please see the full job description at the end of the job ad.
SCHEDULE
READY TO JOIN OUR BIOTECH TEAM?
We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon!
WORK AUTHORIZATION
All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas.
ABOUT CASTLE BIOSCIENCES INC.
At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.
Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.
Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail .
This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
** No third-party recruiters, please
Castle Biosciences Inc. is growing, and we are looking to hire a full-time Clinical Research, Clinical Safety Manager working from our Phoenix, AZ, Friendswood, TX or Pittsburgh, PA office location, with a start date of August 1, 2026.
Why Castle Biosciences?
Exceptional Benefits Package:
- Excellent Annual Salary + 20% Bonus Potential
- 20 Accrued PTO Days Annually + 10 Paid Holidays
- 401K with 100% Company Match up to 6%
- 3 Health Care Plan Options + Company HSA Contribution
- Company Stock Grant Upon Hire
A DAY IN THE LIFE OF AN Clinical Safety Manager
The Clinical Research Safety Manager is responsible for establishing, implementing, and continuously improving clinical research safety processes for a laboratory-developed test (LDT) and medical device organization while ensuring compliance with applicable regulations, Company policies, and Standard Operating Procedures (SOPs). This role serves as the operational safety lead for company-sponsored clinical studies, overseeing safety planning, adverse event management, risk assessments, safety reporting, and regulatory documentation for FDA-regulated LDT, IVD, and medical device studies. The position partners with cross-functional teams to ensure participant safety, regulatory compliance, inspection readiness, and alignment between clinical safety activities, quality systems, and post-market processes. This individual contributor role also supports the development of safety processes, study documentation, and training while providing support as directed by leadership and contributing to the growth of the clinical research safety function.
REQUIRED QUALIFICATIONS
- Bachelor's degree in life sciences, nursing, clinical research, biomedical sciences, regulatory/quality, public health, or related field.
- 5+ years of clinical research, clinical safety, medical device/IVD, diagnostics, regulatory, quality, or related experience in a regulated healthcare environment.
- Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies, including protocol review, safety reporting pathways, IRB/EC interactions, and study documentation.
- Working knowledge of FDA clinical research and medical device requirements, including 21 CFR Parts 803, 812, and 820 and applicable safety/reporting expectations.
- Experience evaluating and documenting adverse events, serious adverse events, unanticipated problems, unanticipated adverse device effects, protocol-defined events, deviations, and safety issues.
*Please see the full job description at the end of the job ad.
SCHEDULE
- Monday-Friday, 40 hours per week, working from our Phoenix, AZ, Friendswood, TX or Pittsburgh, PA office locations.
- Occasional overnight travel, up to 10%, may be required to support site engagement, audits/inspections, study meetings, training, or conferences.
READY TO JOIN OUR BIOTECH TEAM?
We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon!
WORK AUTHORIZATION
All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas.
ABOUT CASTLE BIOSCIENCES INC.
At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.
Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.
Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail .
This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
** No third-party recruiters, please
About Castle Biosciences
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
201 - 500 Employees
Headquarters location
Friendswood, TX, US
Year founded
2008