From clinical trials to regulatory, consulting, and market access, every clinical development ... The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading ...
From clinical trials to regulatory, consulting, and market access, every clinical development ... The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading ...
Manager of Study Start Up
Blue Bell, PA · On-site +1
Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and ...
Manager of Study Start Up
Blue Bell, PA · On-site +1
Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and ...
Study start-up strategy * Enrollment acceleration plans * Site activation timelines * Data flow and ... Clinical Operations (regional teams / RCSMs) * Medical, Regulatory, Biometrics, Supply, etc.
Study start-up strategy * Enrollment acceleration plans * Site activation timelines * Data flow and ... Clinical Operations (regional teams / RCSMs) * Medical, Regulatory, Biometrics, Supply, etc.
Support the execution of Phase I-IV studies including study start-up, site management and clinical operations activities in compliance with principles of ICH-GCP guidelines, SOPs, local laws and ...
Quick apply
Support the execution of Phase I-IV studies including study start-up, site management and clinical operations activities in compliance with principles of ICH-GCP guidelines, SOPs, local laws and ...
Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...
Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...
Senior Clinical Study Manager
Sunnyvale, CA · On-site +1
... start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM IV) / Senior ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...
Senior Clinical Study Manager
Sunnyvale, CA · On-site +1
... start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM IV) / Senior ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...
Senior Clinical Study Manager
Sunnyvale, CA · On-site +1
... start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM IV) / Senior ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...
Senior Clinical Study Manager
Sunnyvale, CA · On-site +1
... start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM IV) / Senior ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...
Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...
Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, ... Location: Remote Responsibilities * Efficiently manage successful execution of global start-up ...
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, ... Location: Remote Responsibilities * Efficiently manage successful execution of global start-up ...
The Senior Director, Study Start-Up Americas with a primary delivery responsibility for North America, will lead the strategic planning and execution of study start-up activities across clinical ...
The Senior Director, Study Start-Up Americas with a primary delivery responsibility for North America, will lead the strategic planning and execution of study start-up activities across clinical ...
Principal Clinical Study Manager
Fremont, CA · Remote
$153K - $255K/yr
Remote Stryker is seeking a Principal Clinical Study Manager to join our Neurovascular Division ... Drive study start-up and execution activities, including contracts, site training, CRF design, data ...
Principal Clinical Study Manager
Fremont, CA · Remote
$153K - $255K/yr
Remote Stryker is seeking a Principal Clinical Study Manager to join our Neurovascular Division ... Drive study start-up and execution activities, including contracts, site training, CRF design, data ...
Clinical Trial Manager - East Coast
Philadelphia, PA · Remote
$95K - $125K/yr
Conducts study start-up activities including the development of protocols, informed consent forms ... Remote
Clinical Trial Manager - East Coast
Philadelphia, PA · Remote
$95K - $125K/yr
Conducts study start-up activities including the development of protocols, informed consent forms ... Remote
Senior Manager, Clinical Operations
Cambridge, MA · On-site +1
... study start-up, conduct and close-out. This role will collaborate with cross-functional study team ... Able to thrive in a remote/virtual environment.
Senior Manager, Clinical Operations
Cambridge, MA · On-site +1
... study start-up, conduct and close-out. This role will collaborate with cross-functional study team ... Able to thrive in a remote/virtual environment.
... start-up and management. Provides solutions to challenges such as enrollment in the clinical study. • Represents the Clinical Affairs Department on cross-functional meetings and projects as needed ...
... start-up and management. Provides solutions to challenges such as enrollment in the clinical study. • Represents the Clinical Affairs Department on cross-functional meetings and projects as needed ...
Clinical Trial Manager
Newark, CA · On-site +1
$136K - $160K/yr
... including study start-up, enrollment, conduct, database lock, statistical outputs (TLFs), and ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...
Clinical Trial Manager
Newark, CA · On-site +1
$136K - $160K/yr
... including study start-up, enrollment, conduct, database lock, statistical outputs (TLFs), and ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...
Clinical Trial Manager
Newark, CA · On-site +1
... including study start-up, enrollment, conduct, database lock, statistical outputs (TLFs), and ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...
Quick apply
Clinical Trial Manager
Newark, CA · On-site +1
... including study start-up, enrollment, conduct, database lock, statistical outputs (TLFs), and ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...
From clinical trials to regulatory, consulting, and market access, every clinical development ... Oversees study start up, closeout and overall life-cycle activities for assigned studies at central ...
From clinical trials to regulatory, consulting, and market access, every clinical development ... Oversees study start up, closeout and overall life-cycle activities for assigned studies at central ...
... start-up and through enrollment and follow-up. The CSM will clearly provide guidance to the ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...
... start-up and through enrollment and follow-up. The CSM will clearly provide guidance to the ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...
Clinical Trial Manager
Newark, CA · On-site +1
$136K - $160K/yr
... including study start-up, enrollment, conduct, database lock, statistical outputs (TLFs), and ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...
Clinical Trial Manager
Newark, CA · On-site +1
$136K - $160K/yr
... including study start-up, enrollment, conduct, database lock, statistical outputs (TLFs), and ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...
Sr. Clinical Study Manager
Sunnyvale, CA · On-site +1
... start-up and through enrollment and follow-up. The CSM will clearly provide guidance to the ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...
Sr. Clinical Study Manager
Sunnyvale, CA · On-site +1
... start-up and through enrollment and follow-up. The CSM will clearly provide guidance to the ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...
Remote Clinical Study Start Up information
See salary details
$22K - $38.7K
1% of jobs
$38.7K - $55.5K
3% of jobs
$55.5K - $72.2K
7% of jobs
$87.1K is the 25th percentile. Wages below this are outliers.
$72.2K - $88.9K
15% of jobs
$88.9K - $105.6K
9% of jobs
$105.6K - $122.4K
14% of jobs
The median wage is $123.4K / yr.
$122.4K - $139.1K
17% of jobs
$150.9K is the 75th percentile. Wages above this are outliers.
$139.1K - $155.8K
13% of jobs
$155.8K - $172.5K
11% of jobs
$172.5K - $189.3K
7% of jobs
$189.3K - $206K
3% of jobs
$22K
$125.3K
$206K
How much do remote clinical study start up jobs pay per year?
As of Jun 9, 2026, the average yearly pay for remote clinical study start up in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.
What is the difference between Remote Clinical Study Start Up vs Remote Clinical Data Coordinator?
| Aspect | Remote Clinical Study Start Up | Remote Clinical Data Coordinator |
|---|---|---|
| Primary Responsibilities | Planning, site selection, regulatory submissions, site initiation | Data entry, data validation, database management, data quality assurance |
| Required Credentials | Life sciences degree, knowledge of GCP, regulatory knowledge | Life sciences or related degree, familiarity with clinical data systems |
| Work Environment | Collaborates with sponsors, sites, regulatory bodies | Works mainly with data management teams and databases |
| Industry Usage | Involved early in trial setup phases | Involved during data collection and analysis phases |
Remote Clinical Study Start Up focuses on preparing and initiating clinical trials, including site selection and regulatory compliance. In contrast, Remote Clinical Data Coordinator manages and ensures the accuracy of clinical trial data during the study. Both roles require related credentials and work within the clinical research industry, but they operate at different stages of the trial process.
More about Remote Clinical Study Start Up jobs
What cities are hiring for Remote Clinical Study Start Up jobs? Cities with the most Remote Clinical Study Start Up job openings:
What are the most commonly searched types of Clinical Study Start Up jobs? The most popular types of Clinical Study Start Up jobs are:
What states have the most Remote Clinical Study Start Up jobs? States with the most job openings for Remote Clinical Study Start Up jobs include:
What job categories do people searching Remote Clinical Study Start Up jobs look for? The top searched job categories for Remote Clinical Study Start Up jobs are:
- Remote Respiratory Clinical Reviewer
- Remote Chiropractic Clinical Reviewer
- Remote Clinical Nurse Leader
- Remote Director Clinical Quality
- Remote Travel Clinical Documentation Specialist
- Remote Functional Medicine Nurse
- Remote Wvu Medicine Nursing
- Fda Physician
- Remote Clinical Documentation
- Holistic Nurse Coach Remote
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.
Job Summary:
The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading global study start-up and site activation activities in Phase I-III and real-world evidence clinical trials. This team member will also partner closely with CRO teams, internal study stakeholders, KOLs, external vendors,
and site networks to drive top quality, best in class delivery, acceleration and optimization of study start-up, site activation and enrollment milestones. The Senior Manager, Study Start-up provides direct oversight, direction, and support beginning with early study planning, country and site selection, data-driven scenario planning, and enrollment forecasting to ensure predictable and consistent delivery. The Senior Manager, Study Start-up will oversee and ensure the delivery of global (end-to-end) study startup activities (strategy, plans, activities, timelines, and synthesis of study startup insights and presentation to study teams) at program/study level.
The Senior Manager, Study Start-up will serve as an expert across the study start-up, country, and site activation landscape. The Senior Manager, Study Start-up creates project plans for efficient implementation and oversight of appropriate processes, tools, and technologies to accelerate start-up activities. This candidate leads successful study and site activation oversight by removing complexity, conducting proactive risk mitigation, and removing obstacles for sites to successfully activate within study and corporate objectives. The Manager, Study Start-up excels in project management, organizational, and communication skills to clearly share best practices with study teams, CROs, and internal stakeholders across the Clinical Operations organization to deliver consistent application of these practices.
Key Accountabilities:
Skills & Requirements:
#LI-CF1
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.
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.
Job Summary:
The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading global study start-up and site activation activities in Phase I-III and real-world evidence clinical trials. This team member will also partner closely with CRO teams, internal study stakeholders, KOLs, external vendors,
and site networks to drive top quality, best in class delivery, acceleration and optimization of study start-up, site activation and enrollment milestones. The Senior Manager, Study Start-up provides direct oversight, direction, and support beginning with early study planning, country and site selection, data-driven scenario planning, and enrollment forecasting to ensure predictable and consistent delivery. The Senior Manager, Study Start-up will oversee and ensure the delivery of global (end-to-end) study startup activities (strategy, plans, activities, timelines, and synthesis of study startup insights and presentation to study teams) at program/study level.
The Senior Manager, Study Start-up will serve as an expert across the study start-up, country, and site activation landscape. The Senior Manager, Study Start-up creates project plans for efficient implementation and oversight of appropriate processes, tools, and technologies to accelerate start-up activities. This candidate leads successful study and site activation oversight by removing complexity, conducting proactive risk mitigation, and removing obstacles for sites to successfully activate within study and corporate objectives. The Manager, Study Start-up excels in project management, organizational, and communication skills to clearly share best practices with study teams, CROs, and internal stakeholders across the Clinical Operations organization to deliver consistent application of these practices.
Key Accountabilities:
- Responsible for driving global study start-up and site activation activities, milestone oversight, and CRO delivery.
- Develop and deliver the global study startup plan by partnering with the CRO Study Startup team.
- Lead development of procedures to enhance internal start-up capabilities and drive efficiencies to align with Trial Delivery Optimization goals.
- Guide study teams through conduct and delivery of key startup activities within timelines that contribute to operational planning/decisions resulting in predictable delivery for achieving R&D goals.
- Oversee the analysis of clinical trial data and its application to conduct accurate study startup forecasts.
- Collaborate with internal Feasibility experts to drive rapid, accurate, and data-driven study startup forecasts, benchmarking assumptions, scenarios and accurate planning.
- Develop creative processes, methodologies, data and technologies to ensure ongoing delivery of valued Study Startup Services.
- Participate in early, global, strategic study planning to ensure corporate goals and timelines for study start-up and site activation are accurate and achievable; ensure CRO commitment to all study deliverables and timelines.
- Partner with CRO to ensure efficient start-up processes and reporting to deliver best in practice country and site activations.
- Work directly with internal study team members and CRO counterparts to progress site activations efficiently and as per targeted milestones; facilitates timely resolution of site-level issues by utilizing in-country intel and expertise to remove or prevent roadblocks
- Tracks and reports relevant KPIs and metrics including local country and site level cycle times to support process improvement and overall operational/business reporting to accelerate site activation
- Oversee consistent application of appropriate study start-up standards and processes to deliver high quality, cost effective clinical studies in line with local operational, legal and regulatory requirements
- Build and maintain study start-up, country and site activation best practices.
- Support the recruitment and performance of junior staff; provide guidance for effective prioritization, problem identification and solving resulting in improved strategic drug development operational efficiency
Skills & Requirements:
- Bachelor's Degree in Science or related discipline required.
- Significant (8+ years) previous experience gained with a CRO or biopharmaceutical company working on multinational clinical studies.
- Considerable (5+ years) managing operational aspects of clinical studies.
- Significant experience in leading global study start-up and site activation activities is required.
- Must have experience working with external CROs and cross functional teams.
- Broad-based experience in clinical development including clinical trial conduct, Study Start-up and feasibility, country and site selection and patient retention and recruitment.
- Knowledge of GCP and a good understanding of the processes associated with clinical operations, study management and monitoring, and local regulatory requirements.
#LI-CF1
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.
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