To lead the process of clinical project feasibility during standalone feasibility (awarded ... Collecting data from data assets as well as country associates, site level Investigators, and KOL ...
To lead the process of clinical project feasibility during standalone feasibility (awarded ... Collecting data from data assets as well as country associates, site level Investigators, and KOL ...
Associate Director, Clinical Science
Cambridge, MA · On-site
$175 - $226/hr
The Associate Director, Clinical Science is responsible for the planning, execution and operational ... Support the design and implementation of early and late-stage clinical projects and ensure that the ...
Associate Director, Clinical Science
Cambridge, MA · On-site
$175 - $226/hr
The Associate Director, Clinical Science is responsible for the planning, execution and operational ... Support the design and implementation of early and late-stage clinical projects and ensure that the ...
To lead the process of clinical project feasibility during standalone feasibility (awarded ... Collecting data from data assets as well as country associates, site level Investigators, and KOL ...
Quick apply
To lead the process of clinical project feasibility during standalone feasibility (awarded ... Collecting data from data assets as well as country associates, site level Investigators, and KOL ...
This role is for a Clinical Associate who has experience managing budgets and forecasting spend for clinical projects. CRO experience is a nice to have, but clinical and financial experience is a ...
This role is for a Clinical Associate who has experience managing budgets and forecasting spend for clinical projects. CRO experience is a nice to have, but clinical and financial experience is a ...
Associate Director, Drug Product - CMC
Boston, MA · On-site
$140K - $195K/yr
... clinical, project management, legal, sourcing, supply chain, quality and regulatory, as well as ... Work Location The (Associate) Director, Drug Product, CMC role is a based in the US, with ...
Associate Director, Drug Product - CMC
Boston, MA · On-site
$140K - $195K/yr
... clinical, project management, legal, sourcing, supply chain, quality and regulatory, as well as ... Work Location The (Associate) Director, Drug Product, CMC role is a based in the US, with ...
Therapeutic Area Biomarker Director - Cardiovascular and Metabolism
Cambridge, MA · On-site
$186 - $345/hr
You will be a core member of CVM clinical project teams, engaged in Translational Data Science ... 150 associates with expertise in all aspects of biomarker science i.e. genetics, genomics ...
New
Therapeutic Area Biomarker Director - Cardiovascular and Metabolism
Cambridge, MA · On-site
$186 - $345/hr
You will be a core member of CVM clinical project teams, engaged in Translational Data Science ... 150 associates with expertise in all aspects of biomarker science i.e. genetics, genomics ...
New
You will be a core member of CVM clinical project teams, engaged in Translational Data Science ... 150 associates with expertise in all aspects of biomarker science i.e. genetics, genomics ...
You will be a core member of CVM clinical project teams, engaged in Translational Data Science ... 150 associates with expertise in all aspects of biomarker science i.e. genetics, genomics ...
You will be a core member of CVM clinical project teams, engaged in Translational Data Science ... 150 associates with expertise in all aspects of biomarker science i.e. genetics, genomics ...
You will be a core member of CVM clinical project teams, engaged in Translational Data Science ... 150 associates with expertise in all aspects of biomarker science i.e. genetics, genomics ...
You will be a core member of CVM clinical project teams, engaged in Translational Data Science ... 150 associates with expertise in all aspects of biomarker science i.e. genetics, genomics ...
You will be a core member of CVM clinical project teams, engaged in Translational Data Science ... 150 associates with expertise in all aspects of biomarker science i.e. genetics, genomics ...
The Manager, Planning Lead will attend clinical project meetings to gather relevant information ... Must work effectively with global work associates. * Ability to interact effectively at high levels ...
The Manager, Planning Lead will attend clinical project meetings to gather relevant information ... Must work effectively with global work associates. * Ability to interact effectively at high levels ...
The Manager, Planning Lead will attend clinical project meetings to gather relevant information ... Must work effectively with global work associates. * Ability to interact effectively at high levels ...
The Manager, Planning Lead will attend clinical project meetings to gather relevant information ... Must work effectively with global work associates. * Ability to interact effectively at high levels ...
Associate Director, Global Submission Management
Boston, MA · On-site
$163.20 - $244.80/hr
## Associate Director, Global Submission ManagementApplylocations: Boston, MAtime type: Full ... clinical project management* Experience managing routine, regional, and lifecycle regulatory ...
Associate Director, Global Submission Management
Boston, MA · On-site
$163.20 - $244.80/hr
## Associate Director, Global Submission ManagementApplylocations: Boston, MAtime type: Full ... clinical project management* Experience managing routine, regional, and lifecycle regulatory ...
Project manage early phase clinical trials * Assist a tenured Project Manager with registration clinical trials * Mentor and assist in the training of project associates * Perform other duties as ...
Project manage early phase clinical trials * Assist a tenured Project Manager with registration clinical trials * Mentor and assist in the training of project associates * Perform other duties as ...
We are currently seeking anEpic Clinical Subject Manager & Project Manager to join our Healthcare ... Supervise associates and senior associates by reviewing work quality, providing coaching, assigning ...
We are currently seeking anEpic Clinical Subject Manager & Project Manager to join our Healthcare ... Supervise associates and senior associates by reviewing work quality, providing coaching, assigning ...
Sr. Associate/Manager Project Management & Operations
Waltham, MA · On-site
$146K - $161K/yr
Job Title: Sr. Associate/Manager - Project Management & Operations Location: Waltham, MA - Hybrid ... Some experience in drug development in functions such as clinical pharmacology, translational ...
Sr. Associate/Manager Project Management & Operations
Waltham, MA · On-site
$146K - $161K/yr
Job Title: Sr. Associate/Manager - Project Management & Operations Location: Waltham, MA - Hybrid ... Some experience in drug development in functions such as clinical pharmacology, translational ...
Associate Director, Global Submission Management
Boston, MA · Hybrid
$163K - $244K/yr
The Associate Director, Global Submission Management (GSM) is responsible for the strategic ... clinical project management * Experience managing routine, regional, and lifecycle regulatory ...
Associate Director, Global Submission Management
Boston, MA · Hybrid
$163K - $244K/yr
The Associate Director, Global Submission Management (GSM) is responsible for the strategic ... clinical project management * Experience managing routine, regional, and lifecycle regulatory ...
Clinical Trial Associate
Waltham, MA · On-site
$75K - $140K/yr
Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly ... Demonstrated multi-tasking and project management skills. Skyhawk Therapeutics is committed to pay ...
Clinical Trial Associate
Waltham, MA · On-site
$75K - $140K/yr
Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly ... Demonstrated multi-tasking and project management skills. Skyhawk Therapeutics is committed to pay ...
Associate Director, Global Submission Management
Boston, MA · On-site
$163K - $244K/yr
The Associate Director, Global Submission Management (GSM) is responsible for the strategic ... clinical project management * Experience managing routine, regional, and lifecycle regulatory ...
Associate Director, Global Submission Management
Boston, MA · On-site
$163K - $244K/yr
The Associate Director, Global Submission Management (GSM) is responsible for the strategic ... clinical project management * Experience managing routine, regional, and lifecycle regulatory ...
Clinical Trial Associate
Waltham, MA · On-site
$75K - $140K/yr
Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly ... Demonstrated multi-tasking and project management skills. Skyhawk Therapeutics is committed to pay ...
Clinical Trial Associate
Waltham, MA · On-site
$75K - $140K/yr
Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly ... Demonstrated multi-tasking and project management skills. Skyhawk Therapeutics is committed to pay ...
Sr. Associate/Manager Project Management & Operations
Waltham, MA · On-site
$146K - $161K/yr
Job Title: Sr. Associate/Manager - Project Management & Operations Location: Waltham, MA - Hybrid ... Key Responsibilities • Support Clinical Pharmacology and Nonclinical program execution by ...
Sr. Associate/Manager Project Management & Operations
Waltham, MA · On-site
$146K - $161K/yr
Job Title: Sr. Associate/Manager - Project Management & Operations Location: Waltham, MA - Hybrid ... Key Responsibilities • Support Clinical Pharmacology and Nonclinical program execution by ...
Clinical Project Associate information
See Massachusetts salary details
$13.91 - $18.14
3% of jobs
$18.14 - $22.36
18% of jobs
$23.20 is the 25th percentile. Wages below this are outliers.
$22.36 - $26.59
20% of jobs
The median wage is $29.15 / hr.
$26.59 - $30.81
15% of jobs
$30.81 - $35.04
11% of jobs
$35.04 - $39.26
4% of jobs
$42.85 is the 75th percentile. Wages above this are outliers.
$39.26 - $43.48
5% of jobs
$43.48 - $47.71
8% of jobs
$47.71 - $51.93
6% of jobs
$51.93 - $56.16
6% of jobs
$56.16 - $60.38
3% of jobs
$13
$34
$60
How much do clinical project associate jobs pay per hour?
What is a clinical project associate?
What are the typical responsibilities of a clinical project associate?
What are the key skills and qualifications needed to thrive as a clinical project associate?
What is the difference between Clinical Project Associate vs Clinical Research Coordinator?
| Aspect | Clinical Project Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree often required; certifications like CCRP beneficial | Bachelor's degree in health or related field; certifications like CCRP common |
| Work Environment | Typically works with project teams, sponsors, and CROs in clinical trial settings | Works directly with patients, investigators, and site staff at clinical trial sites |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research sites |
| Search & Comparison Intent | High overlap in responsibilities and certifications | Similar roles but more patient-facing |
The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.
What are the most commonly searched types of Clinical Project jobs in Massachusetts?
The most popular types of Clinical Project jobs in Massachusetts are:
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For Clinical Project Associate jobs in Massachusetts, the most frequently searched job titles are:
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The top searched job categories for Clinical Project Associate jobs in Massachusetts are:
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Cities in Massachusetts with the most Clinical Project Associate job openings:

Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 8 days ago
Job description
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: Feasibility Informatics Manager
Role Summary:
To serve as a technical feasibility strategy expert, leading and managing the process of clinical project feasibility in support of proposal teams by assisting Business Development with the generation of cost proposals, providing input and advice relating to operational strategy, and supporting client interactions and long-term strategic partnerships.
To perform as a technical expert in the feasibility strategy development process for internal (e.g., to Business Development Operations) and external clients (e.g., Sponsors), providing strategic input. This includes, but is not limited to:
Serving as an expert resource to project teams for feasibility strategy and informatics services (e.g., feasibility during rescue situations).
Providing support during bid defense (or potential preferred partner) meeting preparation and attending/presenting at bid defense (or potential preferred partner) meetings.
Providing handover to awarded site identification (site ID) team of all relevant feasibility strategy proposed during RFP process, followed by End of Site ID analysis to be performed.
To lead the process of clinical project feasibility during standalone feasibility (awarded) projects by managing and being accountable for the delivery of all awarded projects assigned to the individual. This includes, but is not limited to, accountability for all recommendations for next steps with assessment of risks and strategies to manage risks to the project delivery.
Responsibilities:
Recognize, exemplify, and adhere to ICON's values (Collaboration, Integrity, Inclusion, and Agility) which center around our commitment to people, clients, and performance.
Recognize the importance of and create a culture of process improvement with a focus on streamlining our processes, adding value to our business and meeting client needs. This includes participation in active sharing of FIM learning across therapeutic teams with a purpose to improve strategic feasibility support and outputs (e.g., leveraging resources and tools, slide development, user-acceptance testing for tools).
Travel (approximately 20%) domestic and/or international as needed.
The FM will maintain communication and relationships between all relevant parties to ensure that available intelligence is utilized to deliver optimal, data-driven feasibility strategy solutions. Relevant parties include, but are not limited to: Proposal team members, Project Managers/Strategy Leads, Patient Recruitment & Retention Specialists, Site Identification Managers/Leads, Therapeutic Experts, Therapeutically Aligned clinical teams (as assigned), Business Development Associates, Sponsors, Quality Assurance Associates, and other internal/external experts.
In performing the above essential functions, the remit includes, but is not limited to:
Preparation of feasibility data by:
Collecting data from data assets as well as country associates, site level Investigators, and KOL interviews when required.
Determining site profile.
Developing appropriate feasibility strategies, including approach and management for standalone feasibilities.
Providing full documentation in the proposal that may include incidence/prevalence, treatment practices, reimbursement practices, competitive landscape, enrollment trend analysis, etc.
Collaborating with Patient Recruitment, Start-up, and other teams as needed.
Ensuring feasibility data is fully evaluated to determine risks to project delivery and that any risks identified are appropriately escalated and solutions planned/discussed within the feasibility strategy (e.g., alternative scenario).
Transitioning all pre-award generated data (including strategy) to the Site ID Manager/Lead (with involvement of awarded project team) upon award.
Preparing internal project information to support ad hoc requests for information (e.g., early engagement, pre-award, post-award).
Conduct of evidence-based feasibility by:
Establishing viability of proposed project through interrogation of internal and external performance metrics (e.g., previous feasibility data, Industry intelligence, EMR/EHR and RWE data) and resources to establish demographics and data on patient populations.
Ensuring all collected data is high-quality, accurate, and fully documented in the ICON feasibility business systems.
Performing accurate and correct data analysis and interpretation to support feasibility strategy solutions.
Preparation for and attendance at bid defense meetings (by phone or in person) by:
Supporting and/or presenting strategic project planning.
Performing as a functional lead with accountability for delivery of high-quality feasibility standalone services (awarded/contracted) by:
Initiating, conducting, coordinating, analyzing, and reporting feasibility studies as contracted on time and on budget (managing staff resources).
Meeting Sponsor objectives and expectations.
Coordinating with the Site ID Lead per RACI.
Developing appropriate country and site selection strategies and analyzing/interpreting results to provide protocol feedback and to make appropriate country and site recommendations based on objective analysis (e.g., ranking).
Documenting and tracking feasibility study results.
What you need:
Master's Degree
6-9 years of experience in a Clinical Research environment
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 requesthere.
Are you a current ICON Employee? Please click here to apply