Consulting Hybrid up to 2 Days Onsite Full time South San Francisco California United States Consulting On Demand Talent About This Role RGP is seeking a Clinical Trials Manager Consultant to lead ...
Consulting Hybrid up to 2 Days Onsite Full time South San Francisco California United States Consulting On Demand Talent About This Role RGP is seeking a Clinical Trials Manager Consultant to lead ...
... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...
... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...
Clinical Trials Manager-B
Stamford, CT · On-site
... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...
Clinical Trials Manager-B
Stamford, CT · On-site
... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...
... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...
... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...
$77K - $116K/yr
Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400119 Surgery-Cancer Control ... The Manager, Clinical Trials Projects, leads and oversees the Project Management Team for the URCC ...
$77K - $116K/yr
Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400119 Surgery-Cancer Control ... The Manager, Clinical Trials Projects, leads and oversees the Project Management Team for the URCC ...
Four (4) or more years of full-time experience in clinical research involving sponsored clinical trials. Proficient in ONCOR Clinical Trials Management System. Bilingual in Spanish. Brief Description ...
Four (4) or more years of full-time experience in clinical research involving sponsored clinical trials. Proficient in ONCOR Clinical Trials Management System. Bilingual in Spanish. Brief Description ...
Assistant Director for Clinical Trials
Stony Brook, NY · On-site
$85K - $100K/yr
Four (4) or more years of full-time experience in clinical research involving sponsored clinical trials. Proficient in ONCOR Clinical Trials Management System. Bilingual in Spanish. Brief Description ...
Assistant Director for Clinical Trials
Stony Brook, NY · On-site
$85K - $100K/yr
Four (4) or more years of full-time experience in clinical research involving sponsored clinical trials. Proficient in ONCOR Clinical Trials Management System. Bilingual in Spanish. Brief Description ...
Four (4) or more years of full-time experience in clinical research involving sponsored clinical trials. Proficient in ONCOR Clinical Trials Management System. Bilingual in Spanish. Brief Description ...
Four (4) or more years of full-time experience in clinical research involving sponsored clinical trials. Proficient in ONCOR Clinical Trials Management System. Bilingual in Spanish. Brief Description ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
$64K - $96K/yr
Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400119 Surgery-Cancer Control ... The Clinical Trials Project Manager II for NCORP is responsible for leading the planning ...
$64K - $96K/yr
Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400119 Surgery-Cancer Control ... The Clinical Trials Project Manager II for NCORP is responsible for leading the planning ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
One (1) year of full-time human research experience. Knowledge of medical terminology. Preferred Qualifications: Experience with coordinating multiple clinical trials. Experience coordinating ...
One (1) year of full-time human research experience. Knowledge of medical terminology. Preferred Qualifications: Experience with coordinating multiple clinical trials. Experience coordinating ...
This full-time faculty position is based in Manhattan and offers the opportunity to lead and expand NYU's rapidly growing portfolio of clinical trials in diabetes, obesity, and related metabolic ...
This full-time faculty position is based in Manhattan and offers the opportunity to lead and expand NYU's rapidly growing portfolio of clinical trials in diabetes, obesity, and related metabolic ...
Clinical Trials Registered Nurse, Cardiology, Research Clinical Trials, Full Time, Day
$45.52 - $56.90/hr
This position is onsite and part of the Valley Clinical Trials Research Program, focusing on ... It is a full-time, day shift role, Monday through Friday, with hours from 8:00 AM to 4:30 PM or 8 ...
Clinical Trials Registered Nurse, Cardiology, Research Clinical Trials, Full Time, Day
$45.52 - $56.90/hr
This position is onsite and part of the Valley Clinical Trials Research Program, focusing on ... It is a full-time, day shift role, Monday through Friday, with hours from 8:00 AM to 4:30 PM or 8 ...
One (1) year of full-time human research experience. Knowledge of medical terminology. Preferred Qualifications: Experience with coordinating multiple clinical trials. Experience coordinating ...
One (1) year of full-time human research experience. Knowledge of medical terminology. Preferred Qualifications: Experience with coordinating multiple clinical trials. Experience coordinating ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
Three (3) years of full-time experience negotiating and/or administering a variety of research ... Experience in clinical trials contracts negotiations. Brief Description of Duties: This role ...
Full Time Labcorp Clinical Trials information
See salary details
$49K - $61.7K
3% of jobs
$61.7K - $74.5K
13% of jobs
$79.6K is the 25th percentile. Wages below this are outliers.
$74.5K - $87.2K
22% of jobs
The median wage is $98K / yr.
$87.2K - $99.9K
14% of jobs
$99.9K - $112.6K
16% of jobs
$118.2K is the 75th percentile. Wages above this are outliers.
$112.6K - $125.4K
16% of jobs
$125.4K - $138.1K
7% of jobs
$138.1K - $150.8K
6% of jobs
$150.8K - $163.5K
2% of jobs
$163.5K - $176.3K
0% of jobs
$176.3K - $189K
0% of jobs
$49K
$107.3K
$189K
How much do full time labcorp clinical trials jobs pay per year?
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Cities with the most Full Time Labcorp Clinical Trials job openings:
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States with the most job openings for Full Time Labcorp Clinical Trials jobs include:
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 5 days ago
Job description
Consulting
Hybrid up to 2 Days Onsite
Full time
South San Francisco California United States
Consulting
On Demand Talent
About This Role
RGP is seeking a Clinical Trials Manager Consultant to lead the execution of clinical trials, ensuring compliance with protocols, SOPs, GCPs, and regulatory requirements. As the Clinical Trials Manager, you will provide leadership to study teams, CROs, and vendors, oversee study budgets and forecasts, monitor trial spend against plans, and ensure effective financial stewardship of clinical programs.
What You Will Work On
- Manage end-to-end clinical trial execution, ensuring compliance with protocols, GCPs, SOPs, and regulatory standards.
- Oversee CROs and vendors, including selection, contracting, budgeting, performance management, and issue escalation.
- Monitor study metrics, enrollment progress, timelines, and risks to drive successful trial delivery.
- Partner with Clinical Development, Regulatory, Legal, Finance, investigators, and key opinion leaders to support study execution.
- Provide operational and technical leadership for clinical documents, trial planning, and process improvements.
- Drive Clinical Operations best practices, functional initiatives, and continuous improvement efforts.
- Support domestic and international study activities through regular site, investigator, and vendor engagement.
What You Will Bring
- BS/BA degree with 10+ years of experience leading global, multi-site clinical trials across ophthalmology, neurology, rare disease, and drug development programs.
- Expertise in clinical development, FDA/EMA regulations, ICH-GCP compliance, and global study execution.
- Proven leadership of Clinical Operations teams, including direct management, mentoring, and staff development.
- Extensive experience selecting, negotiating, and overseeing CROs and external vendors.
- Strong financial acumen with responsibility for study budgets, forecasting, and financial reporting.
- Effective collaborator with investigators, key opinion leaders, vendors, and executive stakeholders.
What You Can Expect
- An inspirational place for you to do your best work, be engaged in meaningful ways, and continually develop the skills, competencies and qualities that set our team apart.
- Compensation commensurate with your qualifications, experience, and other factors including geographic location, market and operational factors.
- Total Rewards include: Medical, Dental, Vision, Life Insurance, Disability Insurance, 401(k) Savings Plan, Employee Stock Purchase Plan, Professional Development Program, Paid Time Off and Paid Sick Time (in geographies where legally required).
What We Do
At RGP, we're creating a future where businesses produce their best work without constraints. We've built a global network of over 2,600 experts across four regions, providing a comprehensive suite of solutions across on-demand talent, next-generation consulting, and outsourced services to support organizations at every stage of their growth journey. Trusted by Fortune 100 companies and emerging disruptors alike, we challenge conventional ways of working, drive growth, and pave the way for long-term success through bold innovation and fearless collaboration.
Our values guide everything we do and strengthen our commitment to people. By combining smart processes, human-centered design, and advanced technology, we celebrate our team's excellence and ensure we grow together. We believe in the power of continuous learning and development to drive both individual and organizational success. It's time to rethink how work gets done. Dare to Work Differently® with RGP.
RGP is proud to be an Equal Opportunity Employer and committed to creating an inclusive environment for all employees. We do not discriminate on the basis of race, color, religion, national origin, gender, pregnancy, sexual orientation, gender identity, age, physical or mental disability, genetic information, veteran status, or any other legally protected trait and encourage all applicants to apply.
About Resources Global Professionals
Sourced by ZipRecruiter
Resources Global Professionals (RGP) is a multinational professional services firm, headquartered in Irvine, California, United States. Founded in 1996, the firm operates in various industries including finance, technology, healthcare, and retail among others. RGP is recognized for its unique approach to consulting, where they help clients transform their businesses through a combination of human talent, industry knowledge, and experience in problem-solving. The company's mission is "to help clients change their businesses from the inside out."
Industry
Business management consulting
Company size
1,001 - 5,000 Employees
Headquarters location
Irvine, CA, US
Year founded
1996