1

Clinical Research Project Manager Jobs in Rome, NY

Research Assistant I (Lab) (4170)

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

next page

Showing results 1-20

Clinical Research Project Manager information

See Rome, NY salary details

$47.3K

$81.5K

$125K

How much do clinical research project manager jobs pay per year?

As of Aug 26, 2026, the average yearly pay for clinical research project manager in Rome, NY is $81,455.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,700.00 and $86,600.00 per year, depending on experience, location, and employer.

What does a clinical research project manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

What are the key skills and qualifications needed to thrive as a clinical research project manager?

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.

What are some common challenges faced by clinical research project managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

What is the difference between Clinical Research Project Manager vs Clinical Research Coordinator?

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch 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.

What cities near Rome, NY are hiring for Clinical Research Project Manager jobs?

Cities near Rome, NY with the most Clinical Research Project Manager job openings:

(Sr) Project Manager, Feasibility Site Activation

Whitesboro, NY โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 hours ago

Posted today


Job description

(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 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:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

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