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Evidence Director Jobs (NOW HIRING)

Cytel

Senior Director, Real World Evidence

Cambridge, MA ยท On-site +1

Serve as thought leader and subject matter expert in real-world evidence. Undertake external visibility engagements (conference presentations, webinars, peer reviewed publications and white papers ...

City of Osage Beach

Evidence Custodian

Osage Beach, MO ยท On-site

$33K - $37K/yr

Supervision Received The Evidence Custodian is responsible to and performs under the direct supervision of the Administrative Lieutenant. Supervision Exercised Not Applicable. Expectation of Job ...

City of Osage Beach, MO

Evidence Custodian

Osage Beach, MO ยท On-site

$33K - $37K/yr

Supervision Received The Evidence Custodian is responsible to and performs under the direct supervision of the Administrative Lieutenant. Supervision Exercised Not Applicable. Expectation of Job ...

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As of Jun 7, 2026, the average yearly pay for evidence director in the United States is $123,955.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,000.00 and $137,000.00 per year, depending on experience, location, and employer.
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Director of Scientific Communications & Evidence Generation

Genetix Biotherapeutics

Somerville, MA โ€ข On-site

Full-time

Medical, Life, Retirement

Posted 19 days ago

Job description

About Genetix Biotherapeutics
At Genetix Biotherapeutics every role has meaning, every team member is respected, and every day is a chance to make a difference. When you join Genetix, you're not just landing a new role, you become part of a company that's pursuing curative gene therapies to give patients and their families more days. We are doers, thinkers and collaborators who embrace and live by our values:
Our innovation is rooted in the diversity of our teams and results are achieved through cooperation and the integration of multiple viewpoints. This is personal and we approach every challenge with radical care.
Position Summary:
The Director of Scientific Communications & Evidence Generation will be responsible for developing a plan for disseminating the company's scientific data (manuscripts, abstracts, posters, presentations); as well as identifying clinical evidence gaps, overseeing non-registrational research, and collaborating with cross-functional teams to generate real-world evidence (RWE), health economics and outcomes research (HEOR), and investigator-sponsored research (ISR) to support product value and safety profiles. This role requires strong scientific writing skills, advance understanding of industry best practices related to publication-related and research-related compliance, as well as cross-functional leadership savvy.
Key Responsibilities:
Scientific Communications & Publication Planning
  • Develop and maintain and 18-month publication plan and lead the publication review process (abstracts, posters, oral presentations, manuscripts, review articles, etc) in compliance with GPP (Good Publication Practice) and ICMJE authorship criteria, as well as data transparency, and fair balance.
  • Utilize innovative formats (micro-learning, interactive pathways, patient-friendly visuals) and ensure accessibility for diverse audiences
  • Maximize the scientific impact of company data via the strategic selection of journals and congresses
  • Collaborate with internal/external expertsand vendors to draft content and ensure the scientific accuracy of all data to be presented.
  • Maintain the enterprise scientific lexicon and core claims matrix; ensure consistency across materials and channels.

Data Generation:
  • Lead the development of an integrated evidence generation plan (IEGP) aligned with overall medical affairs goals to address unmet needs in collaboration with Clinical Development, Regulatory, HEOR, and Commercial teams to avoid duplicative efforts.
  • Evaluate and acquire new data sources (clinical trials, RWD, registries) to support evidence plans.
  • Create processes for synthesizing feedback from various sources, including field insights and advisory boards and analyze the data to uncover trends and actionable insights to guide scientific communication and strategic decision-making designed to effect change.
  • Conceptualize and execute non-promotional education for multidisciplinary audiences (hematology, BMT/transplant, apheresis, transfusion medicine, genetic counseling, nursing), including webinars, symposia, workshops, and digital learning modules.
  • Establish content measurement frameworks (reach, engagement, knowledge lift, practice intent) and continuous improvement loops.
  • Provide operational management for Medical Affairs-led research, including RWE, HEOR, and ISR, including monitoring the contractual commitments of vendors and collaborators to ensure quality and timeline adherence.
  • Ensure all evidence generation activities follow ICH-GCP guidelines, SOPs, and compliance requirements for post-marketing research.

Cross-Functional Partnership
  • Collaborate within Medical Affairs and with Clinical Development, Regulatory, Pharmacovigilance, Commercial, Market Access, and Patient Advocacy to ensure accuracy and balance across communications.
  • Develop and deliver scientific training programs for internal teams (e.g., onboarding for MSLs/field medical; refresher modules on gene therapy mechanisms, safety monitoring, LTFU requirements)..

Associated Responsibilities:
  • Own Med Affairs content as well as related SOPs and work processes.
  • Ensure adherence to policies and procedures via audits.
  • Develop and deliver monthly and quarterly updates to track progress and align on key priorities.
  • Develop and manage department budget
  • Lead or co-lead medical review for scientific materials; partner with Legal/Compliance/Regulatory on clear SOPs and guardrails.

Qualifications:
  • MD, PharmD, PhD in a biomedical field; experience in hematology or Oncology or cell and gene therapy strongly preferred.
  • 8+ years in Medical Affairs/Scientific Communications within biopharma, including publication planning and medical education leadership.
  • Understanding of hemoglobinopathies (SCD, ฮฒ-thalassemia), cell-based gene therapy modalities, safety monitoring (including long-term follow-up), and registry/RWE experience is preferred
  • Experience building omnichannel education programs.
  • Fluency with compliance frameworks (GPP, ICMJE, ACCME, OIG, PhRMA Code) and medical review processes.
  • Exceptional scientific writing, editorial judgment, and stakeholder management; comfortable engaging with KOLs, investigators, and advocacy leaders.

Additional Information
The pay transparency range provided below is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. This role is eligible for an annual bonus and long-term incentive. Actual base salary pay will be based on several factors, including but not limited to experience, skills, relevant education/qualifications, external market, internal equity, and other job-related factors permitted by law.
Genetix's total rewards package also provides employees with a comprehensive and competitive benefits suite to support a variety of employee needs. These benefits include comprehensive health, life and disability insurance, employer-matched 401(k) plan, lifestyle spending account, flexible time-off + paid holidays and winter holiday period, tuition reimbursement & loan repayment assistance, paid parental leave, paid onsite parking, commuter subsidy, and much more.
Pay Transparency
$214,000-$255,000 USD
Genetix is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics.

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