New · posted Oct 31
Azurity Pharmaceuticals · Pharmaceuticals
Senior Clinical Project Manager
- Raleigh, NC
- Hybrid
- Full-time
- Manager
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.
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
What you need
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 Qualificationsnice to have
- 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
The California Consumer Privacy Act regulates privacy rights and consumer protection for residents of California, United States. For details, click here.
The General Data Protection Regulation (GDPR) sets guidelines for the collection and processing of personal information from individuals who live in the European Union (EU).
What you'll do
- 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.
Where you'll work
Raleigh, NCHybridOpen in Maps (opens in a new tab)
More jobs in Raleigh, NCEqual opportunity, accessibility and legal noticesAzurity Pharmaceuticals's statements, word for word
Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
Job intelligence
The context around this role
Live data · October 31, 2026
Salary intelligence
How the pay compares
Manager roles in the US7 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $153,500 | $171,000 | $173,500 |
Comparisons: the base pay employers published on open Clinical Project Management roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Project Management
The general path across 12 open Clinical Project Management roles on Regulatory Jobs, with the titles they carry most. Not Azurity Pharmaceuticals's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 26 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct15
- Collaboration and leadership9
- GMP and compliance5
- Documentation and SOPs5
- Regulatory submissions2
- Data and digital systems2
- Lab testing and methods1
- Investigations and CAPA1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Azurity Pharmaceuticals on Regulatory Jobs
- 4
- Open roles
- 2
- Distinct roles
- 2
- Locations
By discipline
- Regulatory2 50%
- Clinical2 50%
By level
- Manager4 100%
More roles at Azurity Pharmaceuticals
- View role
Senior Clinical Project Manager
Woburn, MA +1 more · HybridManagerPharmaceuticalsSalary not listed
- View role
Senior Manager, Regulatory Affairs
Woburn, MA +1 more · HybridManagerPharmaceuticalsSalary not listed
- View role
Senior Manager, Regulatory Affairs
Raleigh, NC · HybridManagerPharmaceuticalsSalary not listed
Similar Clinical Project Management roles elsewhere
- View role
Clinical Project Manager
IpsenCambridge, MAManagerPharmaceuticals$144K–$200K
Senior Clinical Project Manager at Azurity Pharmaceuticals
Open until filled.