ZipRecruiter

Log In

1

Clinical Development Manager Jobs in Raleigh, NC

Dexian

Clinical Outsourcing Manager

Raleigh, NC · On-site

$95 - $100/hr

... and clinical development activities. This role partners with cross-functional stakeholders ... Outsourcing Management Lead clinical outsourcing strategy for assigned clinical studies and ...

Cellectis

Director, Clinical Quality Assurance

Raleigh, NC · On-site

$190K - $2M/yr

Manage vendor qualifications, audits, and corrective/preventive actions (CAPAs) * Collaborate cross-functionally to integrate quality principles into clinical development and regulatory deliverables

next page

Showing results 1-20

All JobsClinical Development Manager JobsClinical Development Manager Jobs in Raleigh, NC

Clinical Development Manager information

See Raleigh, NC salary details

$28K

$128.4K

$283.2K

How much do clinical development manager jobs pay per year?

As of Jun 29, 2026, the average yearly pay for clinical development manager in Raleigh, NC is $128,435.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,077.00 and $157,069.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Development Manager, and why are they important?

To thrive as a Clinical Development Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a life sciences degree and relevant industry experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Strong leadership, problem-solving, and communication skills distinguish top performers in this role. These skills are vital for ensuring successful clinical trials, regulatory approval, and effective cross-functional collaboration.

How does a Clinical Development Manager typically collaborate with cross-functional teams during a clinical trial?

A Clinical Development Manager works closely with various cross-functional teams, including clinical operations, regulatory affairs, data management, and biostatistics, to ensure the successful execution of clinical trials. They facilitate communication between these departments, align project timelines, and address any operational challenges that arise. By fostering collaboration, they help ensure that studies are conducted in compliance with regulatory standards, data is accurately collected and analyzed, and that project milestones are met on schedule.

What is the difference between Clinical Development Manager vs Clinical Research Associate?

AspectClinical Development ManagerClinical Research Associate
Required CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in life sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple clinical trials, manages teams, and coordinates with stakeholdersMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsagePharmaceutical companies, biotech firms, CROsResearch sites, CROs, pharmaceutical companies

The Clinical Development Manager focuses on overseeing the entire clinical development process, managing teams, and strategic planning. In contrast, the Clinical Research Associate primarily monitors clinical trial sites and ensures compliance. Both roles are essential in clinical research but differ in scope and responsibilities.

What does a Clinical Development Manager do?

A Clinical Development Manager oversees the planning, execution, and management of clinical trials for new drugs or medical devices. They coordinate cross-functional teams, ensure compliance with regulatory requirements, and monitor the progress of studies to ensure timelines and budgets are met. Their work helps bring new therapies to market safely and efficiently by managing all aspects of clinical research from initiation to completion.
What are the most commonly searched types of Clinical Development jobs in Raleigh, NC? The most popular types of Clinical Development jobs in Raleigh, NC are:
What are popular job titles related to Clinical Development Manager jobs in Raleigh, NC? For Clinical Development Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Development Manager jobs in Raleigh, NC look for? The top searched job categories for Clinical Development Manager jobs in Raleigh, NC are:
Clinical Development Manager jobs near you
Infographic showing various Clinical Development Manager job openings in Raleigh, NC as of June 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $128,435 per year, or $61.7 per hour.
Global Clinical Operations Leader / Clinical Trial Manager

Global Clinical Operations Leader / Clinical Trial Manager

Parexel

Raleigh, NC • On-site

Full-time

Posted 4 days ago

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About Parexel
Parexel is a leading global clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry. With more than 22,000 employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care option for anyone anywhere.
We work with focus agility and shared purpose moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking experienced leaders who are motivated by accountability ownership and measurable impact.
About the Role
We are seeking a Global Clinical Operations Leader/Clinical Trial Manager to join our team in a remote position. As a Global Clinical Operations Leader/ Clinical Trial Manager, you will lead the clinical operations strategy and execution of global clinical trials. This role has direct accountability for delivering studies on time within budget and to the highest quality standards while ensuring patient safety and regulatory compliance.
You will serve as the primary clinical liaison to project leadership and sponsor teams coordinating cross functional contributors across regions and time zones. This is a highly visible leadership role suited for individuals who thrive in complex global environments and are comfortable making decisions in ambiguous situations. Success requires strong ownership, the ability to lead without close supervision and a history of delivering clinical trials within a CRO environment.
Key Responsibilities
  • Lead global clinical operations strategy and execution for assigned clinical trials.
  • Drive study startup including site selection, monitoring strategy, and operational planning.
  • Coordinate cross functional teams across geographies ensuring alignment on timelines quality and deliverables.
  • Monitor study progress including recruitment retention data quality and timelines and take corrective action when needed.
  • Identify risks early and implement mitigation and contingency plans.
  • Provide leadership direction and performance feedback to project team members.
  • Function as primary point of contact for sponsors on clinical operations topics.
  • Ensure compliance with ICH GCP regulatory requirements and internal processes.
  • Oversee maintenance and quality of study documentation and central files.
  • Support audits inspections and study closeout activities including database lock and archiving.
  • Provide strategic oversight of the integrated data delivery (IDD) framework and champion a proactive data-quality culture

You will thrive in this role if you bring:
  • Strong leadership decision making and problem-solving skills
  • Demonstrated ability to lead global teams across cultures and time zones
  • Ability to prioritize competing demands and remain accountable for outcomes
  • A proactive mindset with strong ownership and sense of urgency
  • Excellent communication and stakeholder management skills
  • Comfort working in a fast-paced performance driven environment

Required Qualifications
  • Degree in life sciences, nursing, or equivalent clinical research experience
  • Minimum of 5 years of experience leading clinical operations within a CRO environment
  • Proven experience in roles such as Clinical Trial Manager, Clinical Project Manager or Clinical Operations Leader
  • Experience leading complex global or multi-region studies
  • Strong knowledge of ICH GCP regulatory requirements and clinical trial processes
  • Experience coordinating cross functional teams and managing study timelines budgets and quality
  • Proficiency with clinical systems and standard tools such as CTMS, EDC, and eTMF

Preferred Qualifications
  • Prior monitoring experience or strong site engagement background
  • Experience contributing to process improvements or operational excellence initiatives
  • Familiarity with multiple therapeutic areas or late phase studies with priority given to those with Metabolic, Obesity, MASH, Ophthalmology and Dermatology / Immunology

The potential base pay range for this role is competitive and aligned to experience level location and demonstrated expertise. Additional incentives may be available based on performance and role scope.
This role is designed for experienced clinical leaders who are ready to take full ownership of global trial delivery. If you are looking for a position with clear accountability, high expectations and meaningful impact on patient outcomes this is the right opportunity.
#LI-SM1
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
PAREXEL logo

About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

View All PAREXEL Jobs

Apply