Medical Science Liaison (MSL), CNS/Neuropsychiatry (West)

TMAC

$120K — $150K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Advanced degree (PharmD, PhD, MD, NP, PA) or equivalent terminal degree with clinical experience required
  • 2+ years' experience in CNS/Neuropsychiatry required
  • 3-6 years as an MSL, ideally in pre-launch clinical trial settings
  • Expertise in engaging Investigators/KOLs for scientific exchange
  • Willingness to travel up to 50% with overnight stays
  • Knowledge of compliance and regulatory requirements in scientific exchange
  • Strong project management and cross-functional integration skills

Responsibilities

  • Enhance the company's credibility in neuropsychiatric disorders
  • Maintain expertise in neuropsychiatry
  • Support clinical trials by partnering with investigators and site staff
  • Recommend and assist in identifying new clinical trial sites
  • Provide scientific support to investigators and site personnel
  • Identify and address barriers to trial execution
  • Act as a scientific resource in the field for trial-related inquiries
  • Build relationships with KOLs and healthcare professionals

Benefits

  • Home-based role with flexible location options
  • Opportunity to work at the forefront of neuropsychiatric clinical development
  • Engagement in high-impact relationships with leading clinical investigators
  • Environment that promotes cross-functional collaboration
  • Contribution to innovative therapeutic concepts and trial execution
Full Job Description
Medical Science Liaison (MSL), CNS/Neuropsychiatry (West)

Territory: Northeast, 50-70% travel

Location: Home based anywhere in (CA, NV, OR, WA,MN, MT, ID, WY, ND, SD)

Business Unit: Medical Affairs

Reports to: Senior Director, Field Clinical and Medical Programs, TMAC

SUMMARY

Serving as a field resource for the Company, the Medical Science Liaison (MSL) will support the company's neurology/psychiatry Phase II clinical development pipeline. The MSL 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 MSL 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, expanding current therapeutic concepts, and achieving enrollment and retention goals.

Duties and Responsibilities:
  • Strengthen the organization's scientific presence and credibility in neuropsychiatric disorders, including schizophrenia and bipolar depression
  • Maintain deep clinical and scientific expertise within the neuropsychiatric area
  • Partner with investigators and site staff to support clinical trials, ensuring understanding of protocols and patient requirements
  • Identify and recommend new clinical trial sites; support feasibility, site selection, and site initiation activities
  • Provide consistent, compliant scientific support to investigators and site personnel
  • Identify barriers to trial execution and contribute solutions to enhance recruitment and retention
  • Act as a field-based scientific resource, addressing trial-related questions and challenges
  • Build and maintain relationships with key opinion leaders (KOLs) and healthcare professionals
  • Collaborate cross-functionally with medical affairs, clinical development, and operations teams
  • Respond to unsolicited medical information requests in a compliant manner
  • Support scientific meetings, advisory boards, and conference activities

Qualifications:
  • Advanced degree (PharmD, PhD, MD, NP, PA) or equivalent terminal degree with appropriate clinical experience and scientific background required
  • 2+ years' CNS/Neuropsychiatry clinical, academic and/or medical experience required
  • Prior experience as an MSL (3-6 years); preferably with a clinical trial focus in a pre-launch setting required
  • Proven ability to engage Investigators/KOLs in non-promotional, scientific exchange
  • Ability to travel, locally and regionally, up to 50% with overnight stays (car, plane, train)
  • Knowledge of local regulatory requirements and Pharmaceutical Association Codes, including regulations governing compliant scientific exchange
  • Demonstrated ability to integrate and work in cross functional network/matrix
  • Demonstrated project management ability

Salary offers to be determined based on industry experience, education, and therapeutic expertise.

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