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CTI

VP Global Medical Affairs

Covington, KY · On-site +1

Strong network within pharmaceutical and biotech sponsors. * Board Certification. About CTI CTI ... a member of our team will reach out to you directly from an @ctifacts.com email address to guide ...

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How much do biotech boards member jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for biotech boards member in the United States is $17.80, according to ZipRecruiter salary data. Most workers in this role earn between $15.62 and $19.71 per hour, depending on experience, location, and employer.

What are Biotech Boards Members?

Biotech Boards Members are individuals who serve on the board of directors for biotechnology companies or organizations. Their responsibilities include guiding the company's strategic direction, overseeing management performance, ensuring regulatory compliance, and making high-level decisions that affect the company's operations and growth. Members often have backgrounds in science, medicine, business, or law, and their expertise helps steer the organization through the complexities of the biotech industry. They play a crucial role in fundraising, partnerships, and ensuring the company meets its scientific and business objectives.

What are the key skills and qualifications needed to thrive as a Biotech Boards Member, and why are they important?

To thrive as a Biotech Boards Member, you need deep expertise in biotechnology, business strategy, and regulatory compliance, often backed by advanced degrees and executive experience in the life sciences sector. Familiarity with industry-specific regulations, intellectual property management, and financial reporting systems is essential, as well as certifications like board governance training. Outstanding leadership, strategic vision, and collaborative communication are vital soft skills for influencing organizational direction and managing diverse stakeholder interests. These competencies enable board members to guide biotech companies toward sustainable growth, navigate complex markets, and ensure adherence to legal and ethical standards.

What are the main responsibilities of a Biotech Boards Member during quarterly board meetings?

As a Biotech Boards Member, your main responsibilities during quarterly board meetings include reviewing company performance metrics, evaluating progress on research and development projects, and providing strategic guidance on regulatory and market challenges. You will often collaborate with executive leadership to assess funding needs, weigh in on partnership opportunities, and ensure compliance with industry standards. It's also common to participate in discussions about intellectual property, clinical trial updates, and long-term vision planning alongside other board members and senior management.
Infographic showing various Biotech Boards Member job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $37,027 per year, or $17.8 per hour.
Senior Medical Science Liaison (Texas/U.S. Oncology)

Senior Medical Science Liaison (Texas/U.S. Oncology)

Tango Therapeutics

Boston, MA

Other

Posted 14 days ago

Job description

Company Overview

Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.

Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.

This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.

The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts.

Summary 

The Senior MSL is a U.S. field-based role within Medical Affairs, reporting to the Executive Director, Medical Affairs. This role will be a core member of Tango's growing field medical team during a critical phase of development.

The Senior MSL will be responsible for highquality scientific exchange, trial execution support, medical education, and insight generation across priority solid tumor indications, with an initial focus on pancreatic cancer (PDAC), non-small cell lung cancer (NSCLC), and our evolving pipeline programs.

This role is ideal for an individual who wants to operate at the intersection of clinical development, external scientific engagement, and launch readiness in a late-emerging biotech environment, where individual impact is high and scientific accountability matters.

Your role

      Primary Focus: Solid tumors (pancreatic cancer (PDAC), non-small cell lung cancer (NSCLC)

      Scientific Exchange & External Engagement

  • Build and sustain deep, credible relationships with priority investigators, KOLs, and emerging scientific leaders in PDAC and NSCLC
  • Conduct high-quality, fair-balanced scientific exchange in response to unsolicited requests, grounded in a strong understanding of Tango's biology, clinical data, and development strategy
  • Serve as a trusted scientific partner on disease biology, treatment paradigms, and evolving standards of care, particularly in high-unmet-need settings such as PDAC

      Clinical Development & Trial Execution Support

  • Support Tango-sponsored clinical trials, with emphasis on:
    • Site identification and activation
    • Enrollment support and investigator engagement
    • Ongoing scientific dialogue to enhance trial conduct
  • Act as a Medical Affairs bridge between investigators and internal Clinical Development and Clinical Operations teams
  • Contribute field-based perspective to protocol feasibility, study design considerations, and operational execution

      Insight Generation & Strategic Contribution

  • Capture and synthesize high-quality, hypothesis-driven insights from the field related to:
    • Trial design and execution
    • Competitive landscape
    • Future evidence needs
  • Translate insights into actionable feedback that informs Medical Strategy, Clinical Development, and future regulatory and commercialization readiness
  • Contribute to refinement of Tango's core scientific narrative as programs mature and data evolve

      Advisory Boards, Congresses & Scientific Presence

  • Support planning and execution of advisory boards, investigator meetings, and other scientific forums
  • Represent Tango at major medical and scientific congresses relevant to PDAC, NSCLC, and precision oncology
  • Maintain up-to-date knowledge of relevant literature, competitive activity, and guideline evolution

      Cross-Functional Collaboration & Compliance

  • Collaborate closely with Medical Affairs leadership, Medical Content, Clinical Development, Regulatory, and other cross-functional partners
  • Serve as a scientific resource to internal stakeholders
  • Uphold the highest standards of compliance, scientific integrity, and ethical engagement

What You Bring

      Education & Experience

  • 8 years of relevant experience with a bachelor's degree, 6 years with a master's degree, or 3 years with an advanced scientific or medical degree (e.g., PharmD, PhD, MD) Candidates with advanced clinical degrees (e.g., NP, PA) and significant oncology Medical Science Liaison experience will also be considered.
  • Experience in PDAC, GI malignancies, or NSCLC strongly preferred
  • Prior experience supporting clinical-stage or pre-launch oncology assets highly valued

      Skills & Attributes

  • Strong scientific acumen with the ability to engage deeply on complex biology and emerging clinical data
  • Demonstrated strength in insight generation, synthesis, and communication
  • Comfortable operating in a fast-moving, high-accountability biotech environment
  • Excellent collaboration skills across matrixed teams
  • Strong understanding of U.S. clinical research and healthcare environments

      Compliance & Technical Requirements

  • Working knowledge of FDA, OIG, ICH, GCP, PhRMA Code, and applicable compliance standards
  • Commitment to compliant, ethical scientific exchange
  • Proficiency in standard business and field tools (CRM, MS Office, virtual engagement platforms)

Work Environment

  • Field-based role in Texas, with residence required within assigned territory
  • ~ 50% domestic travel expected, with significant time spent with external scientific partners

Why Join Tango Medical Affairs?

  • Be part of a Medical Affairs team built for a transition from mid-stage to late-stage development
  • Contribute directly to trial success, data readiness, and future regulatory and commercialization pathways
  • Expand and establish Tango as a credible clinical scientific leader in precision oncology
  • Work in a lean, collaborative environment where your scientific judgment and execution matter

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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