TMAC
Clinical Trial Liaison CTL Respiratory Central
TMAC, Chicago, Illinois, United States, 60290
Central Territory Includes: IL, MI, OH, KY, WI, IN, TN, MOServing as a field resource for The Medical Affairs Company (TMAC), the
Clinical Trial Liaison (CTL), reporting as Early Clinical Liaison , will represent the Company’s Respiratory Clinical Development program. The CTL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators to support efforts to improve recruitment and activation timelines. The CTL will be responsible for developing and fostering relationships with key stakeholders including clinical investigators and site staff to represent the Company with the goal of improving enrollment. The CTL will engage in scientific exchange with external experts in the Respiratory therapeutic area.Duties and Responsibilities:
Develop, foster, maintain, and manage relationships with key sites, as well as with External Experts and other healthcare professionals.Provide relevant operational, medical, and scientific support, including scientific and educational presentations.Support overall and site recruitment strategy and activities.Assist in implementing site operational strategies and driving site performance.Solicit feedback from the sites and respond to requests for medical or operational information or unsolicited questions or issues raised in a scientific, fair-balanced, compliant manner.Professionally represent the Company at select meetings.Provide regional expertise and site knowledge and support of the study teams with start-up, recruitment, and sponsor oversight activities.Identify key sites where a strategic partnership should be implemented.Qualifications:
Terminal Scientific Degree (examples: PhD, MD, DO, PharmD, PsyD, DNP, B.Sc.), or Master’s degree in Nursing with current APRN licensure.Minimum 1 year of relevant therapeutic and/or clinical trial experience in respiratory specialty therapeutic experience AND/OR minimum of 1 year of relevant pharmaceutical industry experience.Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics.Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded.Fluency in English and in local language in country of residence required.Demonstrates a proactive nature to engage and motivate investigators/clinical trial sites.Knowledge of FDA compliance, GCP guidance and regulatory requirements.Excel in ability to integrate and work in cross functional network.Ability to manage a geographically assigned territory from a home-based office.Willingness to travel within the assigned region is required, 50% or more; overnight travel is required as needed.Valid driver’s license.COVID-19 Vaccination Requirements:
An essential function of this role is being able to support and visit customer’s sites and locations (hospitals, institutions). If such customers or locations have a COVID-19 policy that requires vaccination against COVID-19 or accepts exemptions, you may be asked to provide proof.Salary offers to be determined based on industry experience, education and therapeutic expertise.
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Clinical Trial Liaison (CTL), reporting as Early Clinical Liaison , will represent the Company’s Respiratory Clinical Development program. The CTL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators to support efforts to improve recruitment and activation timelines. The CTL will be responsible for developing and fostering relationships with key stakeholders including clinical investigators and site staff to represent the Company with the goal of improving enrollment. The CTL will engage in scientific exchange with external experts in the Respiratory therapeutic area.Duties and Responsibilities:
Develop, foster, maintain, and manage relationships with key sites, as well as with External Experts and other healthcare professionals.Provide relevant operational, medical, and scientific support, including scientific and educational presentations.Support overall and site recruitment strategy and activities.Assist in implementing site operational strategies and driving site performance.Solicit feedback from the sites and respond to requests for medical or operational information or unsolicited questions or issues raised in a scientific, fair-balanced, compliant manner.Professionally represent the Company at select meetings.Provide regional expertise and site knowledge and support of the study teams with start-up, recruitment, and sponsor oversight activities.Identify key sites where a strategic partnership should be implemented.Qualifications:
Terminal Scientific Degree (examples: PhD, MD, DO, PharmD, PsyD, DNP, B.Sc.), or Master’s degree in Nursing with current APRN licensure.Minimum 1 year of relevant therapeutic and/or clinical trial experience in respiratory specialty therapeutic experience AND/OR minimum of 1 year of relevant pharmaceutical industry experience.Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics.Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded.Fluency in English and in local language in country of residence required.Demonstrates a proactive nature to engage and motivate investigators/clinical trial sites.Knowledge of FDA compliance, GCP guidance and regulatory requirements.Excel in ability to integrate and work in cross functional network.Ability to manage a geographically assigned territory from a home-based office.Willingness to travel within the assigned region is required, 50% or more; overnight travel is required as needed.Valid driver’s license.COVID-19 Vaccination Requirements:
An essential function of this role is being able to support and visit customer’s sites and locations (hospitals, institutions). If such customers or locations have a COVID-19 policy that requires vaccination against COVID-19 or accepts exemptions, you may be asked to provide proof.Salary offers to be determined based on industry experience, education and therapeutic expertise.
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