CrawlJobs Logo

Clinical Trial Liaison

iconplc.com Logo

iconplc

Location Icon

Location:
United States , North Carolina

Category Icon
Category:
IT - Administration

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

Job Description:

As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. Our client is looking for someone to have broad immunology experience, specific preference for dermatology, respiratory and/or allergy experience. Candidate must be located in: NC, OH, IN, KY, MI or IL.

Job Responsibility:

  • Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies
  • Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards
  • Foster strong relationships with study sites and investigators to enhance patient recruitment and retention
  • Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process
  • Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes

Requirements:

  • Bachelor's degree in a relevant field, such as life sciences or healthcare
  • Proven experience in clinical trial enrollment or related roles
  • Strong analytical and problem-solving skills with the ability to interpret complex medical data
  • Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders
  • Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment
  • Broad immunology experience, specific preference for dermatology, respiratory and/or allergy experience
What we offer:
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Additional Information:

Job Posted:
May 04, 2026

Employment Type:
Fulltime
Work Type:
Remote work
Icon
iconplc - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Clinical Trial Liaison

Manager, Clinical Operations, International

Cabaletta is seeking a Manager/Sr Manager, Clinical Operations, International. R...
Location
Location
Germany; Switzerland
Salary
Salary:
Not provided
cabalettabio.com Logo
Cabaletta Bio Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree or advanced degree in life sciences or related field
  • Minimum 4 years of clinical trial management experience including management of study resources, vendors, budgets, supplies, critical path activities, and risk management, within Biotech or pharmaceutical industry or equivalent by experience
  • Cell therapy experience preferred and/or focus complex therapies
  • Fluency in English
  • working proficiency in additional European languages a plus
  • Experience with early phase, complex trials
  • Experience managing Contract Research Organizations and other external vendors
  • Good understanding of European regulatory requirements (EMA, MHRA, etc)
  • Working knowledge of GCP/ ICH regulatory guidelines
  • Extensive knowledge of standard industry practices related to study start-up, site management and monitoring, document management, and clinical supply management
Job Responsibility
Job Responsibility
  • Provide day-to-day clinical project management oversight of the full range of clinical operations activities associated with clinical trial conduct from protocol development, feasibility/capability assessments, initiation, execution, control, and closure
  • Perform hands-on activities not outsourced to vendors, as needed
  • Author study documents and plans such as ICF and study specific plans
  • Provide input and review of site training materials
  • Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate
  • Proactively identify risks and lead team members to mitigate risks in a timely fashion
  • Develop and maintain positive relationships, both internal and external to project, including site personnel (KOLs, PIs, Study Coordinators)
  • Select and manage vendors
  • Perform and document study-level Sponsor Oversight of outsourced clinical activities
  • Execute clinical operations country submission tasks and documents: Review submission pack, coordinate country-specific ethics RFIs, review and update site-specific consent forms
What we offer
What we offer
  • health and retirement
  • PTO
  • stock option plans
Read More
Arrow Right

Medical Science Liaison

As a Medical Science Liaison, you will advance medical science through clinical ...
Location
Location
Algeria , Algiers
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent product knowledge and expertise
  • Outstanding presentation and communication skills in both the local language and English
  • Proven teaching capabilities and an understanding of adult learning concepts
  • Effective critical thinking skills and strategy implementation
  • A broad understanding of the regulatory and healthcare environment in the country/region
  • Excellent organizational skills, resilience, and empathy
  • An MD and/or PhD and/or equivalent healthcare qualifications, preferably with proven MSL experience
  • 2-3 years post-graduate experience within the healthcare industry
  • Clinical trial experience with knowledge of GCP
  • Training in adverse event reporting
Job Responsibility
Job Responsibility
  • Identifies and advances clinical needs, ensuring that we continually meet the evolving requirements of the healthcare community
  • Acts as the primary contact for investigator-initiated trials, facilitating the successful implementation of research initiatives
  • Assists in the development of publication plans to share new findings and insights with the broader medical community
  • Supports the medical manager in the review of promotional materials, ensuring they comply with the highest standards of accuracy and compliance
  • Acts as a liaison with the medical community, including medical professional societies, opinion leaders, investigators, and consultants
  • Supports the medical director/medical manager in collaborating with opinion leaders
  • Provides accurate and balanced medical-scientific education and information on products, therapies, issues, trends, and clinical research
  • Conducts demonstrations and in-services at customer sites
  • Assists in the development of medical-scientific advisory boards, symposia, and educational forums
  • Educates and trains internal staff on products and therapies
  • Fulltime
Read More
Arrow Right

Medical Science Liaison

As a MEDICAL SCIENCE LIAISON in Algeria at Baxter you will play a pivotal role i...
Location
Location
Algeria , Algiers
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent product knowledge and expertise
  • Outstanding presentation and communications skills in both the local language and English
  • Proven teaching capabilities and an understanding of adult learning concepts
  • Effective critical thinking skills and strategy implementation
  • A broad understanding of the regulatory and healthcare environment in the country/region
  • Excellent organizational skills, resilience, and empathy
  • An MD and/or PhD and/or equivalent healthcare qualifications, preferably with proven MSL experience
  • 2-3 years post-graduate experience within the healthcare industry
  • Clinical trial experience with knowledge of GCP
  • Training in adverse event reporting
Job Responsibility
Job Responsibility
  • Identifies and advances clinical needs, ensuring that we continually meet the evolving requirements of the healthcare community
  • Acts as the primary contact for investigator-initiated trials, facilitating the successful implementation of research initiatives
  • Assists in the development of publication plans to share new findings and insights with the broader medical community
  • Supports the medical manager in the review of promotional materials, ensuring they compete with the highest standards of accuracy and compliance
  • Acts as a liaison with the medical community, including medical professional societies, leaders with a point of view, visionaries, investigators, and consultants
  • Supports the medical director/medical manager in collaborating with leaders with a point of view, encouraging relationships that drive innovation and excellence in medical science
  • Provides accurate and fair-balanced medical-scientific education and information on products, therapies, issues, trends, and clinical research
  • Conducts demonstrations and in-services at customer sites to ensure flawless clinical use of products
  • Assists in the development of medical-scientific advisory boards, symposia, and other educational forums
  • Educates and trains internal staff on products, therapies, issues, trends, and clinical research, ensuring our team remains at the forefront of medical knowledge
  • Fulltime
Read More
Arrow Right

Clinical Trial Liaison

As a Clinical Trial Liaison at ICON, you will design and analyse clinical trials...
Location
Location
United States , Raleigh
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a relevant field, such as life sciences or healthcare
  • Oncology experience is required
  • Proven experience in clinical trial enrollment or related roles
  • Strong analytical and problem-solving skills with the ability to interpret complex medical data
  • Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders
  • Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment
Job Responsibility
Job Responsibility
  • Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies
  • Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards
  • Foster strong relationships with study sites and investigators to enhance patient recruitment and retention
  • Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process
  • Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right

Associate Director, Regional Clinical Operations

Associate Director, Regional Clinical Operations. ICON plc is a world-leading he...
Location
Location
United States , Atlanta; Houston; Tampa; Dallas
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum Bachelor’s degree with 5-7 years of experience in Clinical Trial Operations in pharmaceutical / biotechnology industry or Clinical Research Organization, or equivalent, including at least 3 years in a role of primary responsibility for clinical trial execution and management
  • Thorough understanding and experience in global clinical trials in a diverse range of patient populations with preferred experience in both oncology and hematology
  • Direct management experience and supervisory responsibility
  • Demonstrated leadership and management skills
  • Goal oriented, self-starter with proven ability to work independently
  • Good knowledge and experience working with external specialist vendors
  • Excellent interpersonal, organizational, problem-solving, and written/verbal communication skills, confidence, and ability to work effectively with a wide variety of medical, research and administrative personnel
  • Able to proactively identify issues and provide potential solutions for resolution
  • Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines and to established quality standards
  • Proficient in Outlook/Word/Excel/PowerPoint
Job Responsibility
Job Responsibility
  • Accountable for oversight of all assigned studies within the country in accordance with the overall development plan and clinical operations plan and under the direction of the global team (Global Clinical Trial Manager), including adherence to quality, timelines and budget
  • Accountable for planning and executing assigned country study goals and commitments, and as needed, leading, organizing, and participating in regional and/or local meetings and training sessions to implement country-level recruitment plans
  • Develops, builds and maintains optimal relationships with key institutions within the country (i.e. Site Alliance Sites), working closely with the Medical Science Liaisons, Global Site Management and Central Services, and other departments as indicated according to the Site Engagement Strategy
  • Drive the identification and inclusion of sites that have access to and can enroll patients who are from groups that have been historically underrepresented in clinical trials (per FDA Guidance for Industry for Improving Enrollment of Participants from Underrepresented Racial and Ethnic Populations in Clinical Trials)
  • Oversees regional study feasibility, site monitoring performance, quality metrics and all relevant activities for assigned studies
  • Drives evidence-based site recommendations and selection
  • Provides support and training for sites to support diverse recruitment and retention, review, assist and optimize site-level diversity plans as needed, check and challenge progress and coordinate and align central efforts across sponsor and CROs
  • Align local and central initiatives and advise and guide on effective community engagement activities
  • Conduct co-monitoring and site identification visits, as needed
  • Collaborates cross-functionally to build and maintain strong relationships and interaction at the country local level (i.e. Medical Science Liaisons, Medical Monitors, Clinical Scientists, etc.) that directly contribute to key study activities and milestones
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Clinical Monitoring Manager

We are seeking a Clinical Monitoring Manager to oversee in-house Oversight CRAs ...
Location
Location
United States
Salary
Salary:
150000.00 - 170000.00 USD / Year
apogeetherapeutics.com Logo
Apogee Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 8 years of experience as a CRA or related role within the pharmaceutical, biotechnology, or medical device industry
  • Minimum 2 years of experience leading a team of CRAs
  • Recent experience working on respiratory, dermatology and / or gastrointestinal clinical trials a plus
  • Certification as a Clinical Research Associate (CCRA) or equivalent preferred
  • Recent experience working on trials utilizing risk-based monitoring models
  • Strong knowledge of International Council for Harmonization (ICH) guidelines, Good Clinical Practice (GCP), and FDA regulations
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and Smartsheet
  • Experience with EDC systems, electronic trial master files (eTMFs) and other clinical trial databases and systems
  • Strong understanding of clinical trial processes and study conduct
Job Responsibility
Job Responsibility
  • Oversee in-house Oversight CRAs that will oversee CRO CRA’s management of clinical study site activities for Apogee sponsored clinical trials
  • Serve as Apogee’s primary liaison with the in-house CRAs and CRO clinical monitoring team and liaise with clinical study sites
  • Accountable for oversight of clinical monitoring activities from site identification through close out of the study site
  • Responsible for the study deliverables of in-house CRAs on a given study(s)
  • May be responsible for the hiring of in-house CRAs
  • Input into and assist with the development of study documents
  • Oversee development and implementation of project specific processes, tools, and documents
  • Support the training and development of in-house CRAs
  • Oversight of review of monitoring visit reports and metrics
  • Responsible for oversight of CRA review of clinical data
What we offer
What we offer
  • Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
  • Three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
  • Commitment to growing you professionally and providing access to resources to further your development
  • Apogee offers regular all team, in-person meetings to build relationships and problem solve
  • Fulltime
Read More
Arrow Right

Senior Clinical Materials Project Manager

Leads or coordinates cross-functional project/program teams from design to deliv...
Location
Location
United States of America , Rochester
Salary
Salary:
63815.00 - 95723.00 USD / Year
urmc.rochester.edu Logo
University of Rochester
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree with major course works in appropriate health, social science, or biological science field required
  • Minimum 5-10 years of experience, or equivalent combination of education and experience required
  • Clinical trials project management experience preferred
  • Knowledge of Good Manufacturing Practices and Good Clinical Practices, planning, implementation, and coordination of clinical trials
  • Strong communication skills, including written communication
  • Strong presentation, interpersonal and organizational skills, and attention to detail
  • Travel required (up to 5%)
Job Responsibility
Job Responsibility
  • Leads or coordinates cross-functional project/program teams from design to delivery of fully-developed products that are ready for customer use
  • Monitors performance and recommends schedule changes, cost adjustments or resource additions
  • Investigates facts and develops solutions to problems during the design and planning phases
  • Provides timely and accurate information and status updates to functional leaders
  • May be responsible for feasibility studies, field trials management, identifying product gaps, defining product requirements and engaging with customers to understand market needs and trends
  • Directs and oversees the planning, implementation, coordination, and supply chain of clinical supplies to support multi-center clinical trials
  • Plans internal meetings and provides professional direction within the clinical materials service unit team
  • Develop and deliver training programs to support new processes and projects
  • Serves as liaison to study sponsors, clinical coordinating centers, data coordinating centers, clinical trial sites, pharmacy departments, contract research organizations, study principal investigators, study medical monitors, biostatistics department, and administration/fiscal unit
  • Drafts and develops the CMSU’s Clinical Materials Specifications Sheet (CMSS), processing orders, shipping instructions, packing lists/Acknowledgement of Receipts (AOR’s), and study drug handling instructions
  • Fulltime
Read More
Arrow Right

Associate Director, Monitoring Oversight Management

We are seeking an Associator Director, Monitoring Oversight Management, to manag...
Location
Location
United States
Salary
Salary:
180000.00 - 205000.00 USD / Year
apogeetherapeutics.com Logo
Apogee Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 8-10 years of experience as a CRA or related role within the pharmaceutical or biotechnology industry
  • Minimum 5 years of experience leading a team of CRAs
  • Recent experience working on respiratory, dermatology and / or gastrointestinal clinical trials preferred
  • Experience working in Phase I – III clinical trials
  • Recent experience working on trials utilizing risk-based monitoring models
  • Strong knowledge of International Council for Harmonization (ICH) guidelines, Good Clinical Practice (GCP) and FDA regulations
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and Smartsheet
  • Experience with EDC systems, electronic trial master files (eTMFs) and other clinical trial databases and systems
  • Strong understanding of clinical trial processes and study conduct
Job Responsibility
Job Responsibility
  • Manage Apogee’s Oversight CRAs who will oversee the performance of CRO monitoring and site management related activities for Apogee sponsored clinical trials
  • Support contract Oversight CRAs globally
  • Serve as Apogee’s primary liaison with the in-house Oversight CRAs and Lead CRAs
  • Contribute to building a culture of team, site and patient centricity
  • Contribute to monitoring related process development, continuous evaluation of monitoring related resourcing, and the development and implementation of risk-based monitoring strategies
  • Leadership of Oversight CRAs globally driving the team to ensure study deliverables are met with efficiency and quality
  • Responsible for hiring in-house Oversight CRAs
  • Assist with creation, review and revision of departmental SOPs and policies
  • Lead, conduct, and document regular meetings with Oversight CRA team and with individual CRAs
  • Assist with creation and delivery of department initiatives, improvement plans and/or training
What we offer
What we offer
  • Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
  • Three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
  • Commitment to growing you professionally and providing access to resources to further your development
  • Apogee offers regular all team, in-person meetings to build relationships and problem solve
  • Fulltime
Read More
Arrow Right