Overall Study Conduct: Hold primary accountability for the operational planning, management, and ... Clinical Data Integration & Workflow Management * Data Integrity & Flow: Collaborate closely with ...
Overall Study Conduct: Hold primary accountability for the operational planning, management, and ... Clinical Data Integration & Workflow Management * Data Integrity & Flow: Collaborate closely with ...
System VP Ambulatory Surgery Development
$106.03 - $148.44/hr
Develop business cases, conduct feasibility studies for new builds (site analysis, design, volume ... Execution & Integration Oversight: Manage the transition from concept to execution, supporting ...
System VP Ambulatory Surgery Development
$106.03 - $148.44/hr
Develop business cases, conduct feasibility studies for new builds (site analysis, design, volume ... Execution & Integration Oversight: Manage the transition from concept to execution, supporting ...
Develop and refine clinical development plans, including study synopses, protocols, and integrated development strategies for new indications * Provide clinical and scientific leadership to cross ...
Develop and refine clinical development plans, including study synopses, protocols, and integrated development strategies for new indications * Provide clinical and scientific leadership to cross ...
Senior/Executive Medical Director, Clinical Development (New Indications)
South San Francisco, CA · On-site
Develop and refine clinical development plans, including study synopses, protocols, and integrated development strategies for new indications * Provide clinical and scientific leadership to cross ...
Senior/Executive Medical Director, Clinical Development (New Indications)
South San Francisco, CA · On-site
Develop and refine clinical development plans, including study synopses, protocols, and integrated development strategies for new indications * Provide clinical and scientific leadership to cross ...
Senior/Executive Medical Director, Clinical Development (New Indications)
South San Francisco, CA · On-site
$300 - $400/hr
... study synopses, protocols, and integrated development strategies for new indications · Provide clinical and scientific leadership to cross‑functional study teams, ensuring alignment on program ...
New
Senior/Executive Medical Director, Clinical Development (New Indications)
South San Francisco, CA · On-site
$300 - $400/hr
... study synopses, protocols, and integrated development strategies for new indications · Provide clinical and scientific leadership to cross‑functional study teams, ensuring alignment on program ...
New
Develop and refine clinical development plans, including study synopses, protocols, and integrated development strategies for new indications * Provide clinical and scientific leadership to cross ...
Quick apply
Develop and refine clinical development plans, including study synopses, protocols, and integrated development strategies for new indications * Provide clinical and scientific leadership to cross ...
The role will include oversight of design and conduct of FIH and proof of concept studies for new ... of an integrated development plan * Assist and manage a medical writer for full protocol ...
The role will include oversight of design and conduct of FIH and proof of concept studies for new ... of an integrated development plan * Assist and manage a medical writer for full protocol ...
Author and review technical protocols, study reports, investigation and scientific presentations ... Support clinical readiness by developing or integrating rapid analytical tools (e.g., endotoxin ...
Author and review technical protocols, study reports, investigation and scientific presentations ... Support clinical readiness by developing or integrating rapid analytical tools (e.g., endotoxin ...
Senior Director Clinical Development - Early Development Team Leader (EDTL)
Jersey City, NJ · On-site
The role will include oversight of design and conduct of FIH and proof of concept studies for new ... of an integrated development plan * Assist and manage a medical writer for full protocol ...
Senior Director Clinical Development - Early Development Team Leader (EDTL)
Jersey City, NJ · On-site
The role will include oversight of design and conduct of FIH and proof of concept studies for new ... of an integrated development plan * Assist and manage a medical writer for full protocol ...
Senior Director, Pathology/Toxicology, Non-Clinical Development & Translational Sciences
Princeton, NJ · On-site
Drafting of study protocols, and peer review of studies and reports, until finalization, leading interpretation of data and oral/written communication of results * Support integrated development ...
Senior Director, Pathology/Toxicology, Non-Clinical Development & Translational Sciences
Princeton, NJ · On-site
Drafting of study protocols, and peer review of studies and reports, until finalization, leading interpretation of data and oral/written communication of results * Support integrated development ...
Integrates scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP
Integrates scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP
Integrates scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP
Integrates scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP
System VP Ambulatory Surgery Development
Chicago, IL · On-site
$106.03 - $148.44/hr
Develop business cases, conduct feasibility studies for new builds (site analysis, design, volume ... Execution & Integration Oversight: Manage the transition from concept to execution, supporting ...
System VP Ambulatory Surgery Development
Chicago, IL · On-site
$106.03 - $148.44/hr
Develop business cases, conduct feasibility studies for new builds (site analysis, design, volume ... Execution & Integration Oversight: Manage the transition from concept to execution, supporting ...
... integrated development plans * Drives execution of the clinical development plan, ensuring ... Leads preparation of clinical study synopses and is a major contributor to protocols, major ...
... integrated development plans * Drives execution of the clinical development plan, ensuring ... Leads preparation of clinical study synopses and is a major contributor to protocols, major ...
$106.03 - $148.44/hr
Develop business cases, conduct feasibility studies for new builds (site analysis, design, volume ... Execution & Integration Oversight: Manage the transition from concept to execution, supporting ...
$106.03 - $148.44/hr
Develop business cases, conduct feasibility studies for new builds (site analysis, design, volume ... Execution & Integration Oversight: Manage the transition from concept to execution, supporting ...
Senior Medical Director, Clinical Development, Obesity
San Diego, CA · On-site
$250 - $350/hr
... integrated development plans * Drives execution of the clinical development plan, ensuring ... Leads preparation of clinical study synopses and is a major contributor to protocols, major ...
Senior Medical Director, Clinical Development, Obesity
San Diego, CA · On-site
$250 - $350/hr
... integrated development plans * Drives execution of the clinical development plan, ensuring ... Leads preparation of clinical study synopses and is a major contributor to protocols, major ...
Process Integration Development Engineer
$155K - $219K/yr
Your day-to-day involves designing, optimizing, and implementing integrated process solutions that ... study. * 2+ years of Semiconductor Industry experience in one or more of the following areas:
Process Integration Development Engineer
$155K - $219K/yr
Your day-to-day involves designing, optimizing, and implementing integrated process solutions that ... study. * 2+ years of Semiconductor Industry experience in one or more of the following areas:
Senior Medical Director, Clinical Development, Obesity
San Diego, CA · On-site
$301.10 - $411/hr
... integrated development plans * Drives execution of the clinical development plan, ensuring ... Study Design, Execution & Oversight: Leads preparation of clinical study synopses and is a major ...
Senior Medical Director, Clinical Development, Obesity
San Diego, CA · On-site
$301.10 - $411/hr
... integrated development plans * Drives execution of the clinical development plan, ensuring ... Study Design, Execution & Oversight: Leads preparation of clinical study synopses and is a major ...
... integrated development plans * Drives execution of the clinical development plan, ensuring ... Leads preparation of clinical study synopses and is a major contributor to protocols, major ...
... integrated development plans * Drives execution of the clinical development plan, ensuring ... Leads preparation of clinical study synopses and is a major contributor to protocols, major ...
... studies in the US. Duties: The responsibilities will vary based on products' life cycles, but will ... Create clinical development strategy and high-level integrated development plan with a team after ...
... studies in the US. Duties: The responsibilities will vary based on products' life cycles, but will ... Create clinical development strategy and high-level integrated development plan with a team after ...
Integrated Development Studies information
See salary details
$29K - $33.7K
7% of jobs
$33.7K - $38.5K
8% of jobs
$42.6K is the 25th percentile. Wages below this are outliers.
$38.5K - $43.2K
11% of jobs
$43.2K - $47.9K
14% of jobs
The median wage is $50.4K / yr.
$47.9K - $52.6K
19% of jobs
$52.6K - $57.4K
13% of jobs
$58.8K is the 75th percentile. Wages above this are outliers.
$57.4K - $62.1K
12% of jobs
$62.1K - $66.8K
8% of jobs
$66.8K - $71.5K
4% of jobs
$71.5K - $76.3K
3% of jobs
$76.3K - $81K
1% of jobs
$29K
$53.4K
$81K
How much do integrated development studies jobs pay per year?
What is the difference between Integrated Development Studies vs Urban Planning?
| Aspect | Integrated Development Studies | Urban Planning |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Development Studies, Social Sciences, or related fields | Bachelor's or Master's in Urban Planning, Geography, or Civil Engineering |
| Work Environment | Community development projects, NGOs, government agencies | Municipalities, government departments, consulting firms |
| Industry Usage | International development, social programs, policy analysis | City design, land use, infrastructure planning |
Integrated Development Studies focuses on holistic community and social development, often working with NGOs and international agencies. Urban Planning concentrates on designing and managing urban spaces and infrastructure. While both fields involve development, Integrated Development Studies emphasizes social and economic aspects, whereas Urban Planning centers on physical space and infrastructure design.
What types of projects do professionals in integrated development studies typically work on, and how does interdisciplinary collaboration factor into their daily responsibilities?
What is integrated development studies?
Is a degree in development studies worth it?
What are the key skills and qualifications needed to thrive as an integrated development studies professional, and why are they important?
What are the career options with integrated development studies?
What jobs can I get with an integrated development studies degree?

Job description
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
The Vice President, Clinical Development Operations provides strategic leadership and operational oversight for the execution of clinical studies dedicated to evidence generation across the Tempus portfolio. This role is primarily responsible for ensuring that all evidence-generating clinical development studies are conducted with the highest standards of quality, on time, within budget, and in full compliance with global regulatory requirements. The VP will focus on driving operational excellence to deliver robust clinical data that supports product validation, regulatory submissions, and clinical evidence goals.
Key Responsibilities
Strategic & Clinical Trial Leadership
- Overall Study Conduct: Hold primary accountability for the operational planning, management, and execution of clinical trials designed for clinical evidence generation.
- Metric-Driven Performance: Drive performance against key trial metrics, including site activation, patient enrollment, data quality, budget adherence, and alignment with corporate goals and regulatory requirements.
- Operational Excellence: Develop and implement optimized operational strategies to enhance trial efficiency, reduce complexity, and accelerate data delivery timelines.
- Resource & Budget Management: Actively participate in budget planning, financial forecasting, and resource allocation for the evidence generation operations unit to ensure optimal performance.
- Data Integrity & Flow: Collaborate closely with Biostatistics and Data Management teams to ensure the timely, accurate, and high-quality flow of trial data into the clinical database, facilitating efficient data cleaning, analysis, and database lock.
- Cross-Functional Collaboration: Interact closely and establish seamless workflows with cross-functional leaders to ensure that clinical trial data from all sources is accurately captured and reconciled.
Cross-Functional Leadership & Team Management
- Team Leadership: Lead, mentor, and develop a high-performing operations team capable of managing a focused portfolio of clinical evidence generation studies.
- Stakeholder Alignment: Serve as the primary operational leader for evidence generation trial conduct, ensuring tight alignment and communication with Clinical Development, Regulatory Affairs, Project Management, and other key stakeholders.
Quality & Regulatory Compliance
- GCP Compliance: Ensure all evidence-generation trial activities are conducted in strict accordance with Good Clinical Practice (GCP), ICH guidelines, and global regulatory standards.
- Inspection Readiness: Maintain a constant state of inspection readiness for all evidence-generation clinical trials and support senior leadership during regulatory authority inspections (e.g., FDA).
Requirements
- Bachelor's degree in a scientific, life sciences, or healthcare discipline required; advanced degree (MS, PhD, PharmD) preferred.
- 13+ years of progressive clinical trial operations experience within pharma, biotech, or medical device sectors, with a distinct focus on managing trials for clinical evidence generation.
- 5+ years managing and building high-performing clinical operations teams.
- Deep, demonstrable knowledge of GCP, ICH guidelines, and experience defending clinical data/sites during regulatory authority inspections (e.g., FDA).
- Proven track record of partnering successfully with Biostatistics, Data Management, and Medical Directors to achieve timely database locks.
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#LI-REMOTE
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.