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Clinical Program Development Jobs in Virginia (NOW HIRING)

... clinical innovation and program development within the neonatal service line • Collaborate with hospital leadership and academic partners to expand neonatal services • Participate in teaching ...

... Drive clinical innovation and program development within the NICU Collaborate with hospital leadership and Virginia Tech Carilion School of Medicine Participate in teaching for medical students ...

$75K - $90K/yr

Program Development & Implementation: * Play a key role in the development and implementation of the clinical model for mental health services within skilled nursing facilities. * Establish program ...

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Showing results 1-20

Clinical Program Development information

See Virginia salary details

$30.2K

$82.9K

$145.5K

How much do clinical program development jobs pay per year?

As of Jun 5, 2026, the average yearly pay for clinical program development in Virginia is $82,872.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,700.00 and $91,000.00 per year, depending on experience, location, and employer.

What is clinical program development?

Clinical program development involves designing, implementing, and evaluating healthcare programs that improve patient outcomes and operational efficiency. Professionals in this field collaborate with medical staff, administrators, and stakeholders to identify needs, develop protocols, and ensure compliance with regulatory standards. Their work often includes project management, data analysis, and ongoing quality improvement. The goal is to create effective clinical services that meet both patient and organizational objectives.

What is the difference between Clinical Program Development vs Clinical Research Coordinator?

AspectClinical Program DevelopmentClinical Research Coordinator
CredentialsTypically requires a degree in health sciences, public health, or related fields; certifications like CCRP or RAC are commonRequires a bachelor's degree in health, nursing, or related fields; certifications like CCRP or CCRC are often preferred
Work EnvironmentWorks in healthcare organizations, pharmaceutical companies, or research institutions focusing on program planning and implementationWorks in clinical trial sites, hospitals, or research centers managing participant coordination and data collection
Employer & Industry UsageUsed by healthcare providers, biotech firms, and research organizations to develop and oversee clinical programsUsed by research sites, hospitals, and academic institutions to manage clinical trial activities

While both roles involve clinical research, Clinical Program Development focuses on designing and managing entire clinical programs, whereas Clinical Research Coordinators handle the day-to-day operations of clinical trials. Understanding these differences helps professionals choose the right career path or job focus within the clinical research industry.

What are some common challenges faced when developing new clinical programs, and how can someone in this role address them?

Developing new clinical programs often involves navigating regulatory requirements, securing stakeholder buy-in, and aligning multidisciplinary teams. A key challenge is ensuring that program design meets both patient needs and organizational goals while staying compliant with healthcare standards. Success in this role requires strong project management skills, effective communication, and the ability to adapt to shifting priorities. Collaborating closely with clinicians, administrators, and external partners is essential to anticipate barriers and implement solutions that support sustainable program growth.

What are the key skills and qualifications needed to thrive in Clinical Program Development, and why are they important?

To thrive in Clinical Program Development, you need expertise in healthcare management, program evaluation, and clinical best practices, often supported by a degree in healthcare administration or a related field. Familiarity with data analytics tools, electronic medical records systems, and quality improvement methodologies is typically required. Strong leadership, collaboration, and strategic planning skills help professionals excel in designing and implementing effective clinical programs. These competencies ensure the creation of programs that enhance patient outcomes, improve operational efficiency, and comply with regulatory standards.
What are popular job titles related to Clinical Program Development jobs in Virginia? For Clinical Program Development jobs in Virginia, the most frequently searched job titles are:
What cities in Virginia are hiring for Clinical Program Development jobs? Cities in Virginia with the most Clinical Program Development job openings:
Infographic showing various Clinical Program Development job openings in Virginia as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $82,872 per year, or $39.8 per hour.
Associate Director, Clinical Operations Program Lead (COPL)

Associate Director, Clinical Operations Program Lead (COPL)

BioSpace, Inc.

Richmond, VA • On-site, Remote

$153K - $241K/yr

Full-time

Dental, Vision, Life, Retirement, PTO

Posted 3 days ago


Job description

Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
OBJECTIVES:
Develop and lead the program-level operational strategy and planning on assigned programs in close collaboration with our strategic partners and other vendors.
Represent Clinical Operations at the Global Program Team (GPT) and partner with Global Clinical Lead to lead the Clinical Sub Team (CST) accountable for the development and execution of the CDP.
Provide program-level sponsor's operational oversight of our strategic partners and other vendors to ensure the effective execution of the clinical studies on time, with high quality and within agreed budget.
Accountabilities
Accountable to the GPT for the translation of the CDP into an optimal operational strategy and plan; ensures assessment of various scenarios operational for optimal execution of the CDP. Maintain close communication with the Global Program Leader and Global Clinical Lead to ensure expectations and activities are aligned.
On assigned clinical programs, develop and lead the clinical program operational strategy in close collaboration with the Clinical Operations Managers (COMs), strategic partners, CROs, and other vendors.
Serve as the point of escalation for the COMs for issues that can't be resolved at the study level. Collaborate with COMs and cross‐functional counterparts to oversee the performance of activities assigned to our strategic partners, CROs, and other vendors.
Responsible for budget planning and accountable for external spend related to clinical program execution. Works closely with COMs, Global Program Manager (GPM), and Finance to ensure on a regular basis that budgets, enrolment, and gaiting are accurate.
Responsible for participating in strategic cross‐functional initiatives for process and/or business improvements.
Communicates program status and issues to ensure timely decision‐making by senior management.
May participate in Business Development/in‐licensing/alliances evaluations by providing operational due diligence.
Review and provide expert clinical operations input into clinical documents related to the drug development process and into preparation for key regulatory meetings as appropriate.
Leads Clinical Operations aspects of inspection readiness activities and acts as subject matter expert during regulatory inspections.
Lead or participate in cross‐functional strategic initiatives and process improvement.
Actively seek new ways of working more efficiently to meet the needs of clinical development.
Demonstrate advanced Takeda Leadership Behaviors and act as a role model for Takeda's values.
Education, Experience, Knowledge And Skills
Education: Bachelor's degree or international equivalent required, Life Sciences preferred. Advanced degree is highly desirable.
Experience: 10+ years' experience in pharmaceutical industry and/or clinical research organization, including 7+ years clinical study/project management. Experience must include early phase clinical studies/Phase 2 studies or later phase global programs. Experience in more than one therapeutic area is highly desired. Expertise in global regulatory and compliance requirements for clinical research, including but not limited to US CFR, EU CTD, and ICH GCP. Awareness of local country requirements is also required.
Skills
Demonstrated excellence in program management, including scenario assessment, risk assessment and contingency planning
Demonstrated excellent matrix leadership and communication skills
Able to influence without authority
Excellent teamwork, communication, organizational, interpersonal, conflict resolution and problem‐solving skills
Entrepreneurial and innovative; takes measured risks; thinks outside the box; challenge the status quo
Pragmatic and willing to drive and support change
Is comfortable with ambiguity
Embody a culture of continual improvement and innovation; promote knowledge sharing
Fluent business English (oral and written)
Travel Requirements
Requires up to 10 % travel, including overnight and international travel to other Takeda sites, strategic partners, and therapeutic area required travel.
Takeda Compensation And Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location
Massachusetts - Virtual
U.S. Base Salary Range
$153,600.00 - $241,340.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short‐term and/ or long‐term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short‐term and long‐term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well‐being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
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BioSpace logo

About BioSpace

Sourced by ZipRecruiter

BioSpace is a renowned leader in the life sciences industry, based in Urbandale, IA, US. Its primary business revolves around delivering crucial career-focussed news, job hunting tools, and career-oriented resources to professionals in the pharmaceutical, biotechnology, and healthcare sectors. Since its inception, BioSpace has been dedicated to offering the most comprehensive scope of life science job opportunities throughout the United States with its Hotbed Maps. These uniquely branded regional maps highlight various dynamic biotech clusters across the nation. The company's mission is to empower the progression of the life sciences sector by connecting organisations and professionals to necessary resources and information.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Urbandale, IA, US

Year founded

1985