U.S. Bankruptcy Court - District of CT
Head of Medical Affairs
U.S. Bankruptcy Court - District of CT, Boston, Massachusetts, us, 02298
At Viridian, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team’s expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets.
Reporting to the Chief Medical Officer, the Head of Medical Affairs will be responsible for providing strategic leadership for all Medical Affairs related activities through the development and execution of the Medical Affairs strategy and tactics that are aligned with corporate goals, priorities and objectives. The ideal candidate will have a strong background in autoimmune disorders, coupled with a proven track record in Medical Affairs leadership.
Key responsibilities include, but are not limited to external stakeholder engagement, operational excellence/compliance, scientific integrity/communication and strategic leadership.
This role is based in our Waltham, MA headquarters. Our office-based employees are required to work in the office three (3) days a week.
Responsibilities (including, but not limited to):
Lead cross-functional initiatives with R&D, regulatory, commercial, and market access teams
Guide therapeutic area strategies and ensure scientific alignment across regions
Ensure scientific integrity and accuracy in all medical communications, publications, and promotional material Build strong relationships and partnerships with the scientific and medical community including collaboration, support and management of corporate office and field-based team members to support successful implementation of Medical Affairs plan
Development and/or oversight of the scientific platform across therapeutic areas including evidence generation plan
Develop and execute plans for dissemination of medical and scientific information including data from clinical research, medical education programs (e.g., advisory boards, symposia) and medical conferences
Develop and oversee the management of a system to track, manage and respond to unsolicited requests for medical inquiries across therapeutic areas
Develop and implement a data sharing policy and process
Build, lead, train and oversee appropriately sized field-based and operational medical affairs teams
Partner with Viridian’s commercial team to ensure appropriate complaint field-based activities
Ensure all medical activities comply with global regulatory requirements and ethical standards
Champion a culture of compliance and scientific excellence including leading internal audits and risk assessments related to medical affairs operations
Collaborate with clinical development teams to define real-world evidence and post-marketing study needs to support product adoption and expansion
Contribute to early-stage clinical development by shaping clinical programs, ensuring scientific relevance, and aligning with patient and market needs
Provide strategic input to ensure medical insights are integrated into payer strategies, health economics, and outcomes research (HEOR) plans
Develop and oversee process for review and approval of Investigator Initiated Studies
Oversee the review and approval of grants, including ACCME accredited CME programs, and sponsorships in compliance with internal policies and/or procedures and external guidelines
Develop and execute strategic Phase 3b/4 trials
Identify strategies and tactics to support clinical development and clinical operations on the execution of clinical trials (e.g., site identification, patient recruitment)
Drive a high-performance culture by fostering personal accountability and a commitment for results
Manage the departmental budget
Requirements
MD (preferred), PhD, or PharmD degree with 20+ years of experience, including 10+ years of management level experience in the biotechnology and/or pharmaceutical industry
Proven track record of 1) leading and building a high-performing Medical Affairs organization in a small/medium biotech and 2) strategic and tactical planning for product launch (US and global)
Proven track record of working cross functionally on strategic planning
Direct involvement with full lifecycle development and medical support of successfully marketed biotechnology or pharmaceutical products as applicable
Demonstrated strong written and verbal communication skills
Efficient independent worker with ability to work in a fast paced environment, handle multiple tasks and be effective in a matrix environment
Strong attention to detail
Strong commitment to ethical standards
Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
Ability to travel up to 50% (domestic and international)
The salary range for this position is commensurate with experience
Viridian offers a comprehensive benefits package including:
Competitive pay and stock options for all employees
Competitive medical, dental, and vision plans
Fertility and mental health programs
Short- and long-term disability coverage
Life, Travel and AD&D
401(k) Company Match with immediate company vest
Employee Stock Purchase plan
Generous vacation plan and paid company holiday shutdowns
Various mental, financial, and proactive physical health programs covered by Viridian
Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.
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Reporting to the Chief Medical Officer, the Head of Medical Affairs will be responsible for providing strategic leadership for all Medical Affairs related activities through the development and execution of the Medical Affairs strategy and tactics that are aligned with corporate goals, priorities and objectives. The ideal candidate will have a strong background in autoimmune disorders, coupled with a proven track record in Medical Affairs leadership.
Key responsibilities include, but are not limited to external stakeholder engagement, operational excellence/compliance, scientific integrity/communication and strategic leadership.
This role is based in our Waltham, MA headquarters. Our office-based employees are required to work in the office three (3) days a week.
Responsibilities (including, but not limited to):
Lead cross-functional initiatives with R&D, regulatory, commercial, and market access teams
Guide therapeutic area strategies and ensure scientific alignment across regions
Ensure scientific integrity and accuracy in all medical communications, publications, and promotional material Build strong relationships and partnerships with the scientific and medical community including collaboration, support and management of corporate office and field-based team members to support successful implementation of Medical Affairs plan
Development and/or oversight of the scientific platform across therapeutic areas including evidence generation plan
Develop and execute plans for dissemination of medical and scientific information including data from clinical research, medical education programs (e.g., advisory boards, symposia) and medical conferences
Develop and oversee the management of a system to track, manage and respond to unsolicited requests for medical inquiries across therapeutic areas
Develop and implement a data sharing policy and process
Build, lead, train and oversee appropriately sized field-based and operational medical affairs teams
Partner with Viridian’s commercial team to ensure appropriate complaint field-based activities
Ensure all medical activities comply with global regulatory requirements and ethical standards
Champion a culture of compliance and scientific excellence including leading internal audits and risk assessments related to medical affairs operations
Collaborate with clinical development teams to define real-world evidence and post-marketing study needs to support product adoption and expansion
Contribute to early-stage clinical development by shaping clinical programs, ensuring scientific relevance, and aligning with patient and market needs
Provide strategic input to ensure medical insights are integrated into payer strategies, health economics, and outcomes research (HEOR) plans
Develop and oversee process for review and approval of Investigator Initiated Studies
Oversee the review and approval of grants, including ACCME accredited CME programs, and sponsorships in compliance with internal policies and/or procedures and external guidelines
Develop and execute strategic Phase 3b/4 trials
Identify strategies and tactics to support clinical development and clinical operations on the execution of clinical trials (e.g., site identification, patient recruitment)
Drive a high-performance culture by fostering personal accountability and a commitment for results
Manage the departmental budget
Requirements
MD (preferred), PhD, or PharmD degree with 20+ years of experience, including 10+ years of management level experience in the biotechnology and/or pharmaceutical industry
Proven track record of 1) leading and building a high-performing Medical Affairs organization in a small/medium biotech and 2) strategic and tactical planning for product launch (US and global)
Proven track record of working cross functionally on strategic planning
Direct involvement with full lifecycle development and medical support of successfully marketed biotechnology or pharmaceutical products as applicable
Demonstrated strong written and verbal communication skills
Efficient independent worker with ability to work in a fast paced environment, handle multiple tasks and be effective in a matrix environment
Strong attention to detail
Strong commitment to ethical standards
Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
Ability to travel up to 50% (domestic and international)
The salary range for this position is commensurate with experience
Viridian offers a comprehensive benefits package including:
Competitive pay and stock options for all employees
Competitive medical, dental, and vision plans
Fertility and mental health programs
Short- and long-term disability coverage
Life, Travel and AD&D
401(k) Company Match with immediate company vest
Employee Stock Purchase plan
Generous vacation plan and paid company holiday shutdowns
Various mental, financial, and proactive physical health programs covered by Viridian
Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.
#J-18808-Ljbffr