The Medical Affairs Company (TMAC)
Clinical Trial Liaison (CTL), Allergy/Rare Diseases (Nationwide)
The Medical Affairs Company (TMAC), Granite Heights, Wisconsin, United States
Clinical Trial Liaison (CTL), Allergy/Rare Diseases (Nationwide)
Join to apply for the
Clinical Trial Liaison (CTL), Allergy/Rare Diseases (Nationwide)
role at
The Medical Affairs Company (TMAC) .
The Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution.
The CTL provides regional specific insights to support study feasibility, site identification and selection, and patient recruitment and retention initiatives. In collaboration with the study team, the CTL both identifies and helps facilitate resolution of investigator site issues.
Responsibilities
Provide country/regional operational insight into site feasibility and selection and overall patient recruitment strategy
Participate in Clinical Study Team Meetings and Quality Review Meetings where necessary, providing input to study teams on operational issues based on site visits and contacts
Attend and present at investigator meetings, monitor workshops/training
Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams (e.g., feasibility, startup activities, enrolment or escalated study/site issues)
Responsible for review, documentation and follow up of investigator site issues including tracking metrics
Provide sponsor regional operational support and act as point of escalation for investigator sites as appropriate
Participate in Regulatory GCP inspections and/or audits at investigator sites as sponsor representative
Contribute to process improvement initiatives when required
Complete all administrative responsibilities consistent with SOPs and departmental guidelines, including training, field activity documentation, expense reporting, and other assigned tasks
Manage travel and local expenses in accordance with sponsor and TMAC policies
Qualifications and Experience
Minimum Bachelor’s degree; master’s preferred or terminal degree (MD, PhD or PharmD)
6+ years of relevant industry and/or CRO clinical trial experience with site-facing roles
Allergy or Rare Diseases clinical trial experience preferred
Extensive medical and scientific knowledge and clinical development understanding
Excellent communicator of technical and scientific information
Excellent interpersonal skills and demonstrated collaborative as well as independent working style
Ability to build relationships with the external medical community
Proactive and self-motivated, ability to align activities with the clinical development plans (CDPs)
Strong organizational skills with effective time management and prioritization
Working knowledge of ICH/GCP
Computer skills including Excel, Word, and PowerPoint
Willingness to travel frequently within assigned geographical territory, including overnight travel
Valid driver’s license
*Salary offers to be determined based on industry experience, education and therapeutic expertise.
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Clinical Trial Liaison (CTL), Allergy/Rare Diseases (Nationwide)
role at
The Medical Affairs Company (TMAC) .
The Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution.
The CTL provides regional specific insights to support study feasibility, site identification and selection, and patient recruitment and retention initiatives. In collaboration with the study team, the CTL both identifies and helps facilitate resolution of investigator site issues.
Responsibilities
Provide country/regional operational insight into site feasibility and selection and overall patient recruitment strategy
Participate in Clinical Study Team Meetings and Quality Review Meetings where necessary, providing input to study teams on operational issues based on site visits and contacts
Attend and present at investigator meetings, monitor workshops/training
Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams (e.g., feasibility, startup activities, enrolment or escalated study/site issues)
Responsible for review, documentation and follow up of investigator site issues including tracking metrics
Provide sponsor regional operational support and act as point of escalation for investigator sites as appropriate
Participate in Regulatory GCP inspections and/or audits at investigator sites as sponsor representative
Contribute to process improvement initiatives when required
Complete all administrative responsibilities consistent with SOPs and departmental guidelines, including training, field activity documentation, expense reporting, and other assigned tasks
Manage travel and local expenses in accordance with sponsor and TMAC policies
Qualifications and Experience
Minimum Bachelor’s degree; master’s preferred or terminal degree (MD, PhD or PharmD)
6+ years of relevant industry and/or CRO clinical trial experience with site-facing roles
Allergy or Rare Diseases clinical trial experience preferred
Extensive medical and scientific knowledge and clinical development understanding
Excellent communicator of technical and scientific information
Excellent interpersonal skills and demonstrated collaborative as well as independent working style
Ability to build relationships with the external medical community
Proactive and self-motivated, ability to align activities with the clinical development plans (CDPs)
Strong organizational skills with effective time management and prioritization
Working knowledge of ICH/GCP
Computer skills including Excel, Word, and PowerPoint
Willingness to travel frequently within assigned geographical territory, including overnight travel
Valid driver’s license
*Salary offers to be determined based on industry experience, education and therapeutic expertise.
#J-18808-Ljbffr