(Sr) Project Manager, Feasibility Site Activation ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Posted today
Quick apply
(Sr) Project Manager, Feasibility Site Activation ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Posted today
Quick apply
(Sr) Project Manager, Feasibility Site Activation ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Posted today
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
East Syracuse, NY ยท On-site
$43K - $44K/yr
Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study * Develop, coordinate, and implement research and administrative strategies to ...
East Syracuse, NY ยท On-site
$43K - $44K/yr
Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study * Develop, coordinate, and implement research and administrative strategies to ...
East Syracuse, NY ยท On-site
$43K - $44K/yr
Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study * Develop, coordinate, and implement research and administrative strategies to ...
East Syracuse, NY ยท On-site
$43K - $44K/yr
Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study * Develop, coordinate, and implement research and administrative strategies to ...
$70K - $88K/yr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
$70K - $88K/yr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Utica, NY ยท On-site
$70K - $88K/yr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Utica, NY ยท On-site
$70K - $88K/yr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Utica, NY ยท On-site
$75K - $115K/yr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Utica, NY ยท On-site
$75K - $115K/yr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Utica, NY ยท On-site
$70K - $88K/yr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Utica, NY ยท On-site
$70K - $88K/yr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Utica, NY ยท On-site
$50 - $55/hr
... managers and technology developers. The Nursing Solutions Group is involved throughout the trial ... Up to 100% travel, as needed, for study participant visits, project team meetings, and other ...
Utica, NY ยท On-site
$50 - $55/hr
... managers and technology developers. The Nursing Solutions Group is involved throughout the trial ... Up to 100% travel, as needed, for study participant visits, project team meetings, and other ...
... managers and technology developers. The Nursing Solutions Group is involved throughout the trial ... Up to 100% travel, as needed, for study participant visits, project team meetings, and other ...
... managers and technology developers. The Nursing Solutions Group is involved throughout the trial ... Up to 100% travel, as needed, for study participant visits, project team meetings, and other ...
Utica, NY ยท On-site
$50 - $55/hr
... managers and technology developers. The Nursing Solutions Group is involved throughout the trial ... Up to 100% travel, as needed, for study participant visits, project team meetings, and other ...
Utica, NY ยท On-site
$50 - $55/hr
... managers and technology developers. The Nursing Solutions Group is involved throughout the trial ... Up to 100% travel, as needed, for study participant visits, project team meetings, and other ...
Utica, NY ยท On-site
$75 - $115/hr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Utica, NY ยท On-site
$75 - $115/hr
Diversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure ...
Project Manager, Imaging and Cardiac ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...
Quick apply
Project Manager, Imaging and Cardiac ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...
Middleville, NY ยท On-site
$18.25 - $25/hr
Any other matters as assigned by management. KNOWLEDGE & EXPERIENCE Education: * High school diploma or equivalent required Experience: * Prior experience in clinical research is not required but ...
Posted today
Middleville, NY ยท On-site
$18.25 - $25/hr
Any other matters as assigned by management. KNOWLEDGE & EXPERIENCE Education: * High school diploma or equivalent required Experience: * Prior experience in clinical research is not required but ...
Posted today
Liverpool, NY ยท On-site
$71K - $189K/yr
... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...
Liverpool, NY ยท On-site
$71K - $189K/yr
... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...
Liverpool, NY ยท On-site
$71K - $189K/yr
... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...
Liverpool, NY ยท On-site
$71K - $189K/yr
... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...
Utica, NY ยท On-site
$19.25 - $25/hr
The Institute's primary mission is to conduct high quality basic biomedical and clinical research ... projects. Requirements * A recent bachelor's or master's degree in biological sciences or related ...
Utica, NY ยท On-site
$19.25 - $25/hr
The Institute's primary mission is to conduct high quality basic biomedical and clinical research ... projects. Requirements * A recent bachelor's or master's degree in biological sciences or related ...
Utica, NY ยท On-site
$19.75 - $27/hr
The Institute's primary mission is to conduct high quality basic biomedical and clinical research ... projects. Requirements * A recent bachelor's or master's degree in biological sciences or related ...
Utica, NY ยท On-site
$19.75 - $27/hr
The Institute's primary mission is to conduct high quality basic biomedical and clinical research ... projects. Requirements * A recent bachelor's or master's degree in biological sciences or related ...
Utica, NY ยท On-site
$19.75 - $27/hr
The Institute's primary mission is to conduct high quality basic biomedical and clinical research ... projects. Requirements: * A recent bachelor's or master's degree in biological sciences or related ...
Quick apply
Utica, NY ยท On-site
$19.75 - $27/hr
The Institute's primary mission is to conduct high quality basic biomedical and clinical research ... projects. Requirements: * A recent bachelor's or master's degree in biological sciences or related ...
$19.75 - $27/hr
The Institute's primary mission is to conduct high quality basic biomedical and clinical research ... projects. Requirements * A recent bachelor's or master's degree in biological sciences or related ...
$19.75 - $27/hr
The Institute's primary mission is to conduct high quality basic biomedical and clinical research ... projects. Requirements * A recent bachelor's or master's degree in biological sciences or related ...
$47.3K - $54.4K
4% of jobs
$54.4K - $61.5K
9% of jobs
$66.9K is the 25th percentile. Wages below this are outliers.
$61.5K - $68.5K
15% of jobs
$68.5K - $75.6K
15% of jobs
The median wage is $77.3K / yr.
$75.6K - $82.6K
27% of jobs
$85.4K is the 75th percentile. Wages above this are outliers.
$82.6K - $89.7K
12% of jobs
$89.7K - $96.7K
4% of jobs
$96.7K - $103.8K
4% of jobs
$103.8K - $110.9K
2% of jobs
$110.9K - $117.9K
4% of jobs
$117.9K - $125K
3% of jobs
$47.3K
$81.5K
$125K
| Aspect | Clinical Research Project Manager | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's or higher in life sciences, often with project management certifications | Bachelor's in health sciences or related field, often with clinical research certifications |
| Work Environment | Oversees multiple projects, manages teams, and liaises with sponsors | Conducts daily clinical trial activities, interacts directly with participants and site staff |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Research hospitals, clinics, academic institutions |
The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.
Cities near Rome, NY with the most Clinical Research Project Manager job openings:
Whitesboro, NY โข On-site
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 13 hours ago
Posted today
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Title: Project Manager, FSA
Role Summary:
As a Project Manager, Feasibility and Site Activation (FSA) at ICON, you will be responsible for planning and manage Feasibility and Site Activation (FSA) activities for assigned clinical studies.
What You Will Do:
You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations.
Key responsibilities include:
Developing and managing FSA project plans, timelines, and deliverables for assigned studies.
Coordinating feasibility assessments, country and site recommendations, and start-up strategies in collaboration with functional experts.
Overseeing essential document collection, ethics and regulatory submissions, and site activation milestones.
Tracking progress against timelines and KPIs, proactively identifying risks and implementing mitigation plans.
Serving as the primary FSA contact for internal teams and customers for study-level start-up matters.
Contributing to process improvement and best practice sharing within the FSA project management team.
Your Profile:
You will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent experience.
Strong experience in clinical research with a focus on feasibility, site activation, or start-up project management.
Proven ability to manage project plans, timelines, and cross-functional coordination in a fast-paced environment.
Good understanding of regulatory, ethics, and contractual requirements affecting study start-up.
Excellent communication, organizational, and stakeholder management skills.
Detail-oriented and proactive, with a commitment to quality, predictability, and customer satisfaction.
Willingness to travel as required (approximately 10%)
Title: Senior Project Manager, FSA
Role Summary:
Accountable for driving and accelerating the activation of global investigative sites in line with, or ahead of, the study's contractual timelines, within budgeted resources, with quality output, and exceeding sponsor expectations. Accountable for the overall coordination, implementation and completion of site activation activities for large global or complex projects of work in line with ICON/sponsor SOPs as appropriate, including regulatory/ethics, site contracts, essential documents, and site activations. Interacts with internal teams and stakeholders, as well as sponsor teams and stakeholders, and presents to Exec Management as needed.
Responsibilities:
Recognize, exemplify and adhere to ICON's values , and contribute to the “Own It” culture at ICON
Accountable for driving and accelerating the activation of global investigative sites in line with, or ahead of, the study's contractual timelines, within budgeted resources, with quality output, and exceeding sponsor expectations.
Accountable for the overall coordination, implementation and completion of site activation activities for large global or complex projects of work in line with ICON/sponsor SOPs as appropriate, including regulatory/ethics, site contracts, essential documents, and site activations.
Interacts with internal teams and stakeholders, as well as sponsor teams and stakeholders, and presents to Exec Management as needed.
Lead studies with highest quality standards to exceed customer expectations.
Review study and partnership budgets for proposals and sales as needed.
Drive assigned studies to meet KPIs and delight customers and sites
Act as customer point of contact for assigned studies; resolve study issues and drive exceptional customer delivery
Represent FSA at audits and inspections
Participate in Business Development opportunities to support the growth of the assigned portfolio, function, and/or region/country(ies)
Travel (approximately 10% depending on country structure and direct report levels) domestic and/or international
Responsible for performing activities that are in compliance with applicable corporate and departmental policies, standard operating procedures and operating guidelines and performing other duties as assigned by the management
Act as a mentor where required
What you need:
Bachelor's Degree
3-6 years of experience in a Clinical Research environment
Demonstrate proficient organizational skills and ability to prioritize tasks with minimal management support and oversight.
Exhibits extensive competency in Microsoft Office Suite applications (i.e. Word, Excel, Powerpoint, Outlook).
Completes tasks independently on time and in an efficient manner.
Ability to mentor and train others as needed.
Show confidence in dealing with internal stakeholders.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply