... s)/CRO to ensure accountability, quality, and on time delivery of key project deliverables ... bioanalytical vendors, etc. * Lead study execution team comprised of cross-functional ...
... s)/CRO to ensure accountability, quality, and on time delivery of key project deliverables ... bioanalytical vendors, etc. * Lead study execution team comprised of cross-functional ...
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experience * Experience in biotech, pharma, CRO, or academic translational research settings ...
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experience * Experience in biotech, pharma, CRO, or academic translational research settings ...
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experience * Experience in biotech, pharma, CRO, or academic translational research settings ...
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experience * Experience in biotech, pharma, CRO, or academic translational research settings ...
... bioanalytical vendors, etc. * Lead study execution team comprised of cross-functional ... CRO vendors and ensure study excellence. * Manage clinical development vendors according to vendor ...
... bioanalytical vendors, etc. * Lead study execution team comprised of cross-functional ... CRO vendors and ensure study excellence. * Manage clinical development vendors according to vendor ...
... bioanalytical vendors, etc. * Lead study execution team comprised of cross-functional ... CRO vendors and ensure study excellence. * Manage clinical development vendors according to vendor ...
Quick apply
... bioanalytical vendors, etc. * Lead study execution team comprised of cross-functional ... CRO vendors and ensure study excellence. * Manage clinical development vendors according to vendor ...
Senior Research Associate, Biodistribution
Durham, NC · On-site
$100 - $125/hr
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experienceExperience in biotech, pharma, CRO, or academic translational research settings ...
Senior Research Associate, Biodistribution
Durham, NC · On-site
$100 - $125/hr
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experienceExperience in biotech, pharma, CRO, or academic translational research settings ...
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experience * Experience in biotech, pharma, CRO, or academic translational research settings ...
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experience * Experience in biotech, pharma, CRO, or academic translational research settings ...
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experience * Experience in biotech, pharma, CRO, or academic translational research settings ...
... bioanalytical sciences, genetics, biomedical sciences, or a related discipline with 2+ years' related work experience * Experience in biotech, pharma, CRO, or academic translational research settings ...
Manager, Project Management
Durham, NC · On-site
... class bioanalytical services. We are tirelessly committed to our customers by being solution ... Knowledge in science with relevant regulations for Contract Resource Organization (CRO) preferred ...
Manager, Project Management
Durham, NC · On-site
... class bioanalytical services. We are tirelessly committed to our customers by being solution ... Knowledge in science with relevant regulations for Contract Resource Organization (CRO) preferred ...
Manager, Project Management
Durham, NC · On-site
... class bioanalytical services. We are tirelessly committed to our customers by being solution ... Knowledge in science with relevant regulations for Contract Resource Organization (CRO) preferred ...
Manager, Project Management
Durham, NC · On-site
... class bioanalytical services. We are tirelessly committed to our customers by being solution ... Knowledge in science with relevant regulations for Contract Resource Organization (CRO) preferred ...
... class bioanalytical services. We are tirelessly committed to our customers by being solution ... Knowledge in science with relevant regulations for Contract Resource Organization (CRO) preferred ...
Quick apply
... class bioanalytical services. We are tirelessly committed to our customers by being solution ... Knowledge in science with relevant regulations for Contract Resource Organization (CRO) preferred ...
MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports)
Quick apply
MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports)
... Bioanalytical Group. The successful candidate will play a key role in developing and validating ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...
... Bioanalytical Group. The successful candidate will play a key role in developing and validating ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...
... Bioanalytical Group. The successful candidate will play a key role in developing and validating ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...
... Bioanalytical Group. The successful candidate will play a key role in developing and validating ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...
... Bioanalytical Group. The successful candidate will play a key role in developing and validating ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...
... Bioanalytical Group. The successful candidate will play a key role in developing and validating ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...
... Bioanalytical Group. The successful candidate will play a key role in developing and validating ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...
... Bioanalytical Group. The successful candidate will play a key role in developing and validating ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...
Bioanalytical Cro information
See Raleigh, NC salary details
$23.3K - $33.1K
15% of jobs
$36.7K is the 25th percentile. Wages below this are outliers.
$33.1K - $42.9K
28% of jobs
The median wage is $47.9K / yr.
$42.9K - $52.8K
14% of jobs
$52.8K - $62.6K
17% of jobs
$63.7K is the 75th percentile. Wages above this are outliers.
$62.6K - $72.4K
12% of jobs
$72.4K - $82.2K
5% of jobs
$82.2K - $92K
5% of jobs
$92K - $101.8K
3% of jobs
$101.8K - $111.6K
0% of jobs
$111.6K - $121.4K
0% of jobs
$121.4K - $131.2K
1% of jobs
$23.3K
$56.8K
$131.2K
How much do bioanalytical cro jobs pay per year?
As of Sep 9, 2026, the average yearly pay for bioanalytical cro in Raleigh, NC is $56,808.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,500.00 and $67,600.00 per year, depending on experience, location, and employer.
What is a bioanalytical CRO?
Bioanalytical CROs, or Contract Research Organizations, are specialized companies that provide analytical testing services to support pharmaceutical, biotechnology, and medical device development. They focus on analyzing biological samples, such as blood, plasma, or tissue, to quantify drugs, metabolites, or biomarkers. These services are crucial for preclinical and clinical studies, ensuring accurate and reliable data for regulatory submissions. Bioanalytical CROs help companies save time and resources by offering expertise, advanced instrumentation, and compliance with industry regulations.
What skills and qualifications are needed to work in a bioanalytical CRO?
To thrive as a Bioanalytical CRO professional, you need a background in life sciences or chemistry, strong analytical laboratory skills, and often a relevant degree such as a BSc or MSc. Familiarity with technical tools like LC-MS/MS, chromatography software, and compliance with GLP/GCP standards is typically required. Attention to detail, problem-solving abilities, and effective teamwork are crucial soft skills in this field. These skills ensure accurate data generation, regulatory compliance, and successful execution of client-sponsored research projects.
What challenges do bioanalytical CRO professionals face, and how can they be addressed?
Professionals working in bioanalytical CROs often encounter challenges such as managing tight project timelines, ensuring regulatory compliance, and adapting to rapidly changing client requirements. Balancing multiple studies simultaneously requires strong organizational skills and effective communication with both internal teams and clients. To address these challenges, it is important to maintain clear documentation, stay updated on industry best practices, and foster a collaborative team environment to ensure high-quality, reproducible results.
What is the difference between Bioanalytical Cro vs Bioanalytical Scientist?
| Aspect | Bioanalytical Cro | Bioanalytical Scientist |
|---|---|---|
| Credentials | Typically requires a degree in life sciences, pharmacology, or related fields; certifications vary by company | Requires a degree in biology, chemistry, or related fields; advanced degrees preferred |
| Work Environment | Contract research organizations, pharmaceutical companies, or biotech firms; project-based work | Research labs, pharmaceutical companies, or academic settings; more independent research |
| Employer & Industry Usage | Commonly hired for clinical trial support and regulatory studies | Engaged in experimental design, data analysis, and method development |
While both roles require a background in life sciences, a Bioanalytical Cro primarily manages outsourced projects and client communication, whereas a Bioanalytical Scientist focuses on experimental work and data analysis within a lab setting.
What job categories do people searching Bioanalytical Cro jobs in Raleigh, NC look for?
The top searched job categories for Bioanalytical Cro jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Bioanalytical Cro jobs?
Cities near Raleigh, NC with the most Bioanalytical Cro job openings:
Senior Clinical Project Manager
Raleigh, NC • Hybrid
Azurity Pharmaceuticals - US
Full-time
Re-posted 6 days ago
Job description
About the Role
The Senior Clinical Project Manager, Clinical Development is responsible for leading the planning, execution, oversight, and delivery of domestic and/or global postmarketing required clinical trials. The Sr. CPM serves as the operational leader for assigned studies, partnering cross-functionally with Medical/Drug Safety, Regulatory, Data Management, Quality, and external vendors to ensure clinical trials are delivered on time, within budget, and in compliance with applicable regulations and quality standards.
Key Responsibilities
- Lead the operational execution of assigned domestic or global, multi-center late phase clinical trial(s) including oversight of selected vendor(s)/CRO to ensure accountability, quality, and on time delivery of key project deliverables.
- Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ensure delivery on timeline and financial goals are met.
- Initiate and manage request for proposal activities for assigned clinical studies or clinical development vendors, including CROs, specialty lab vendors, bioanalytical vendors, etc.
- Lead study execution team comprised of cross-functional representatives from Regulatory, Drug Safety, Medical, Drug Supply, Data Management, Biostatistics, and Quality to oversee CRO vendors and ensure study excellence.
- Manage clinical development vendors according to vendor oversight plans.
- Oversee all study-level data monitoring activities, reviews monitoring visit reports, and conducts Sponsor oversight monitoring visits as required.
- Responsible for monthly Protocol Deviation (PD) review, including oversight of CRA documentation and collaboration with Medical Monitor for medical review.
- Prepares and/or reviews study-related study plans/documents; reviews site study documents.
- Assist in strategic trial design and protocol writing.
- Strategic country/site selection with program input and ensuring consistency across all clinical projects for therapeutic area.
- Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and applicable SOPs: participates in the planning of quality assurance activities and coordinates resolution of audit findings; ensures audit-ready condition of clinical trial documentation including central clinical files, Trial Master File (TMF), and clinical trial registry submissions.
- Ensure inspection readiness and compliance with ICH-GCP, FDA, EMA, and applicable regulatory requirements.
Required Skills and Experience
- Bachelor's degree in Life Sciences or a related scientific discipline (advanced degree preferred).
- 8+ years of Clinical Trial / Project Management experience within CRO, biotechnology or pharmaceutical organizations.
- Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
- Proven leadership of global clinical studies and cross-functional project teams.
- Strong experience managing CROs, vendors, and external partners.
- Extensive knowledge of ICH-GCP, FDA, EMA, and global clinical trial regulations.
- Excellent communication, leadership, and project management skills.
Preferred Qualifications
- 5+ years' experience of clinical trial management for late phase studies
- Experience with IMP/clinical drug supply logistics, planning, and labeling activities in late phase studies
- Effective communicator who can manage multiple priorities while building strong internal relationships across multiple departments
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