TMAC

Role Description Serving as a field-based extension of the Company, the Senior Medical Science Liaison (Sr. MSL) will represent the Company and their recently approved PCSK9 inhibitor therapy indicated as an adjunct to diet and exercise: to reduce low-density lipoprotein cholesterol (LDL-C) in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia (HeFH). - Engage in meaningful scientific discussions with external stakeholders about the disease state and the scientific evidence supporting the Company’s products/portfolio. - Support and facilitate medical communications and publications (e.g. abstracts, case studies/series, review articles) by acting as a liaison between external stakeholders and the Company’s internal stakeholders. - Assess KOL alignment with the key elements of the scientific platform to inform territory and medical strategy. - Stay abreast of emerging scientific literature/clinical data and translate the data in applicable knowledge exchange. - Collect scientific and clinical insights to support ongoing information/clinical data sharing (i.e. new data, competitive information, insights learned from customers) to optimize communications and coordinated activities across the organization. - Thrive in a small company environment and adapt to the dynamic nature of a growing organization. - Ability to travel, up to 60% of the time. Qualifications - Advanced scientific/clinical degree (MD, DNP, PhD, PharmD, PA or NP) required. - A minimum of 2+ years’ MSL experience in the pharmaceutical industry required. - Dyslipidemia experience required, preferably including PCSK9. - Thorough knowledge of medicine, treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines is preferred. - Demonstrated ability to access and develop relationships with high-level stakeholders. - Ability to effectively communicate scientific content through 1:1 meetings, small group interactions, and in writing. - Must be a strong team player and effectively collaborate with internal departments. Requirements - Territory: East, Central, West. - TMAC is building out a new MSL team on behalf of our client and are seeking candidates located in the United States, ideally near a major airport hub. - Salary offers to be determined based on industry experience, education, and therapeutic expertise. Benefits - #LI-JD1 - #LI-Remote

Role Description 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 countries/regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution. The CTL provides regional and country 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. Duties and 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 - Provides sponsor regional operational support and acts as point of escalation for investigator sites as appropriate - Participate in Regulatory GCP inspections and/or audits at investigator sites as sponsor representative - Complete all administrative responsibilities consistent with SOPs and departmental guidelines including but not limited to required training, field activity documentation, expense reporting, and other assigned tasks - Manage travel and local expenses in accordance with sponsor and TMAC policies Qualifications - Minimum Bachelor’s degree, master’s preferred or terminal degree (MD, PhD or PharmD) - 8+ years relevant industry and/or CRO experience required - Extensive experience in site facing clinical trial operations required - Hem/Onc or Cardio/Metabolic clinical trial experience - 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 relations with the external medical community - Proactive and self-motivated, ability to align activities with the clinical development plans (CDPs) - Strong organizational skills with effective use of time and prioritization - Cross cultural awareness - Fluency in English and in local language in country of residence required - A working knowledge of ICH/GCP - Computer skills including Excel, Word, and PowerPoint - A willingness to travel frequently within assigned geographical territory, including overnight travel. - Valid driver’s license

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description The Medical Science Liaison (MSL) will serve as a liaison to the medical/scientific community and will be responsible for establishing, developing, and maintaining relationships with key stakeholders within the geographic and therapeutic area of coverage. This is a field Medical Affairs position requiring a strong scientific background (technical or clinical experience) as the MSL will be a credible source of clinical/scientific data as well as technical/practical education to practicing clinicians, key opinion leaders (KOL), professional societies, and payers. MSLs are responsible for developing, coordinating, and assuring implementation of corporate scientific imperatives. - Develop relationships with KOLs in the assigned territory based on scientific exchange - Engage in scientific dialog effectively communicating scientific content in response to KOL requests - Assess KOL alignment with the key elements of the scientific platform to inform territory and medical strategy - Develop KOL Advocates and Collaborators within your assigned territory - Compliantly support company sponsored research, investigator-initiated studies, and publications associated with Company product(s) - Stay abreast of emerging scientific literature/clinical data and translate the data in applicable knowledge - Ensure appropriate dissemination of clinical and scientific information regarding FDA approved and pipeline products in a timely, ethical, and customer-focused manner with support of your manager - Respond to MIRFs with an initial contact within 2 days and a full answer within 3 weeks - Collect scientific and clinical insights to support ongoing information/clinical data sharing (i.e. new data, competitive information, insights learned from customer) to optimize communications and coordinated activities across the organization - Respond to all requests for directed insights within the expected timeframe - Participate in advisory board - Contributes scientific content and helps build materials in support of a project or initiative - Understand and practice the Company Values - Must be committed to full compliance with all company SOPs, regulatory requirements, and applicable laws including PhRMA guidelines for field-based personnel - Applicants must possess a valid driver’s license - Ability to travel, up to 60% of the time Qualifications - Advanced scientific degree (MD, PharmD/RPh, DNP, NP, RN, PA) - Cardiovascular, Nephrology, Hepatology, Critical Care, or Emergency Medicine experience - MSL experience not required - Thorough knowledge of medicine, treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines is preferred - Demonstrated ability to access and develop relationships with high-level stakeholders - Ability to effectively communicate scientific content through 1:1 meetings, small group interactions, and in writing - Must be a strong team player and effectively collaborate with internal departments Requirements - Must be committed to full compliance with all company SOPs, regulatory requirements, and applicable laws including PhRMA guidelines for field-based personnel - Applicants must possess a valid driver’s license - Ability to travel, up to 60% of the time