Clinical Scientist
OR · On-site +1
The Clinical Scientist represents Clario scientific expertise at all external meetings. The Clinical Scientist co-leads all assigned projects with Project Management and collaborates ...
OR · On-site +1
The Clinical Scientist represents Clario scientific expertise at all external meetings. The Clinical Scientist co-leads all assigned projects with Project Management and collaborates ...
OR · On-site +1
The Clinical Scientist represents Clario scientific expertise at all external meetings. The Clinical Scientist co-leads all assigned projects with Project Management and collaborates ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
New
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
New
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
Irvine, CA · On-site
About this opportunity - Clinical Scientist Description Clinical Scientist with a strong background in clinical science and medical writing. Experience in clinical evidence and clinical operations ...
Irvine, CA · On-site
About this opportunity - Clinical Scientist Description Clinical Scientist with a strong background in clinical science and medical writing. Experience in clinical evidence and clinical operations ...
Oncology Clinical Scientist (Contractor) This contractor role provides clinical research support within Oncology/Solid Tumors Clinical Development, with a strong focus on protocol development and ...
New
Quick apply
Oncology Clinical Scientist (Contractor) This contractor role provides clinical research support within Oncology/Solid Tumors Clinical Development, with a strong focus on protocol development and ...
New
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist represents Clario scientific expertise at all external meetings. The Clinical Scientist co-leads all assigned projects with Project Management and collaborates ...
The Clinical Scientist represents Clario scientific expertise at all external meetings. The Clinical Scientist co-leads all assigned projects with Project Management and collaborates ...
Irvine, CA · On-site
About this opportunity - Clinical Scientist Description Clinical Scientist with a strong background in clinical science and medical writing. Experience in clinical evidence and clinical operations ...
Irvine, CA · On-site
About this opportunity - Clinical Scientist Description Clinical Scientist with a strong background in clinical science and medical writing. Experience in clinical evidence and clinical operations ...
Seattle, WA · On-site +1
If you're a clinical scientist and clinicaldevelopment professional eager to work on cutting-edge science with a collaborative team and growyour career, this could be the role for you. Key ...
Seattle, WA · On-site +1
If you're a clinical scientist and clinicaldevelopment professional eager to work on cutting-edge science with a collaborative team and growyour career, this could be the role for you. Key ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
Pearl River, NY · On-site
$29/hr
Qualifications The Clinical Scientist will work collaboratively with the clinical lead and team to execute the clinical program(s). Their primary deliverable is to assist in the assist in planning ...
Pearl River, NY · On-site
$29/hr
Qualifications The Clinical Scientist will work collaboratively with the clinical lead and team to execute the clinical program(s). Their primary deliverable is to assist in the assist in planning ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights ...
If you're a clinical scientist and clinicaldevelopment professional eager to work on cutting-edge science with a collaborative team and growyour career, this could be the role for you. Key ...
If you're a clinical scientist and clinicaldevelopment professional eager to work on cutting-edge science with a collaborative team and growyour career, this could be the role for you. Key ...
Director, Clinical Scientist - Rare Kidney Disease Biotech | Boston, MA Hlx is partnering with an emerging, venture-backed biotechnology company developing innovative therapies for rare kidney ...
New
Director, Clinical Scientist - Rare Kidney Disease Biotech | Boston, MA Hlx is partnering with an emerging, venture-backed biotechnology company developing innovative therapies for rare kidney ...
New
$28.37 - $33.22
6% of jobs
$33.22 - $38.07
13% of jobs
$40.21 is the 25th percentile. Wages below this are outliers.
$38.07 - $42.92
14% of jobs
$42.92 - $47.77
11% of jobs
The median wage is $51.27 / hr.
$47.77 - $52.62
9% of jobs
$52.62 - $57.47
18% of jobs
$57.47 - $62.33
2% of jobs
$64.14 is the 75th percentile. Wages above this are outliers.
$62.33 - $67.18
6% of jobs
$67.18 - $72.03
3% of jobs
$72.03 - $76.88
7% of jobs
$76.88 - $81.73
11% of jobs
$28
$54
$81
| Aspect | Weekend Clinical Scientist | Weekend Medical Laboratory Technician |
|---|---|---|
| Credentials | Typically requires a degree in clinical science, biomedical science, or related field; certification may be preferred | Requires a diploma or associate degree in medical laboratory technology; certification often required |
| Work Environment | Hospitals, diagnostic labs, research facilities during weekends | Laboratories, hospitals, clinics during weekends |
| Employer & Industry | Healthcare providers, diagnostic labs, research institutions | Hospitals, diagnostic labs, healthcare facilities |
| Common Search & Comparison | Weekend Clinical Scientist vs Weekend Medical Laboratory Technician |
The Weekend Clinical Scientist and Weekend Medical Laboratory Technician roles both operate in healthcare and diagnostic environments during weekends. The Clinical Scientist typically holds a higher degree and may be involved in interpreting results and research, while the Laboratory Technician focuses on sample processing and testing. Both roles are essential for weekend lab operations, but they differ in responsibilities and required qualifications.

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 14 days ago
Clinical Scientists at Clario, a part of Thermo Fisher Scientific play a critical role in advancing clinical research by ensuring the scientific integrity and successful execution of global clinical trials. In this clientfacing role, you will serve as a trusted scientific partner to sponsors and internal teams, contributing directly to highquality evidence generation that supports lifechanging therapies. If you thrive in a dynamic, collaborative environment and enjoy combining scientific rigor with stakeholder engagement, this role offers the opportunity to make a meaningful impact.
What We Offer
Competitive compensation
Comprehensive medical, dental, and vision coverage
401(k) with company match
Generous paid time off and company holidays
Flexible remote work arrangement within the United States
What You'll Be Doing
Serve as an externalfacing clinical representative with independent scientific responsibility for assigned international clinical trials, acting as a primary point of contact for clinical and scientific matters.
Colead projects with accountability for scientific integrity, ensuring appropriate analyses, issue remediation, and clear communication to sponsors and internal stakeholders.
Participate actively in internal and external project meetings, including sponsor calls and investigator meetings.
Review, monitor, and proactively address studylevel metrics; develop and present study dashboards highlighting data trends, outliers, risks, and mitigation actions.
Resolve clinical quality, data integrity, and trainingrelated issues in alignment with study requirements and Good Clinical Practice (GCP).
Lead calibration of clinical teams, conduct rater training sessions, and implement remediation activities according to studyspecific training plans.
Provide scientific guidance and support to internal teams, sponsors, and external partners using effective communication, influencing, and negotiation skills.
Respond to and resolve external inquiries related to Clario scoring methodologies or clinical feedback.
Coordinate crossfunctional resources to ensure project milestones and deliverables are met.
Contribute to the development of project deliverables, including scale verification, electronic form development, and training materials for inperson or virtual delivery.
Support Business Development activities by providing scientific input for feasibility reviews and RFP responses.
Build and maintain professional relationships with external consultants, key opinion leaders, and clinicians.
Participate in research initiatives and disseminate findings through publications, conferences, or other scientific forums.
Contribute to the development and continuous improvement of work instructions, process guidelines, and SOPs to ensure compliance with SOP and GCP standards.
What We Look For
Bachelor's degree required; graduate degree in life sciences or a related field preferred.
Minimum of five years of experience in the clinical research industry, with prior experience in a CRO or biopharmaceutical environment preferred.
At least three years of experience in a clinical scientist, clinical trial science lead, or similar clientfacing scientific role.
Minimum four years of handson experience with administration and/or training of clinical rating scales and study endpoints.
Experience in neuroscience; whether in education, relevant scales or populations.
Solid understanding of basic and intermediate research methods and statistics.
Demonstrated ability to manage multiple projects in a fastpaced environment.
Proven leadership through influence, with strong problemsolving and independent criticalthinking skills.
Excellent written and verbal communication skills, with experience presenting to diverse and large audiences.
Fluency in English; additional languages are a plus.
Strong knowledge of Good Clinical Practice (GCP).
Ability to travel internationally approximately 10-20% and perform extended computerbased work.
At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It's a cause that unites and inspires us. It's why we come to work-and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring lifechanging therapies to patients faster.
EEO Statement Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
Sourced by ZipRecruiter
1,001 - 5,000 Employees
Princeton, NJ, US
1987