Medical Director (Hematology / Oncology)

Real; Boston (MA); Hybrid; USD 275,520 - 378,840; Part time

Job summary

A leading healthcare organization in Boston is seeking a part-time Medical Director specializing in Hematology/Oncology. This role involves leadership in clinical development and regulatory oversight. Candidates should have an M.D. and experience in the industry. Join to impact innovation in the oncology field with flexible hours. Competitive pay ranging from $200 to $275 per hour.

Qualifications

• 3+ years of industry experience with strong regulatory and clinical development experience.
• Experience with Acute Lymphoblastic Leukemia (ALL).

Responsibilities

• Shape data generation, study designs, and decision-making processes across teams.
• Provide guidance on regulatory preparations and monitor clinical trials.

Skills

Clinical Expertise in Hematology/Oncology

Strategic Leadership

Collaboration and Teamwork

Regulatory and Medical Oversight

Data-Driven Problem Solving

Education

M.D. and board certification in medical Hematology / Oncology

Job description

Medical Director (Hematology / Oncology)

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Medical Director (Hematology / Oncology)

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This range is provided by Real. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$200.00/hr - $275.00/hr

Medical Director Opportunity



Join Our Client's Innovative Hematology Team!

We are excited to announce a rewarding opportunity for a Medical Director to join our client's highly skilled team dedicated to advancing innovation in the Oncology space. Based in Boston, this contract role will focus on late-stage and life cycle management development within the Hematology Program. Our client is a global leader with approved medications in oncology and other therapeutic areas, driven by a mission to address unmet medical needs.

Key Skills for Success

• Clinical Expertise in Hematology/Oncology:
  • M.D. and board certification in medical Hematology / Oncology
  • 3+ years of industry experience with strong regulatory and clinical development experience
  • Acute Lymphoblastic Leukemia (ALL) experience
• Strategic Leadership: Provide insights to shape data generation, study designs, and decision-making processes across cross-functional teams.
• Collaboration and Teamwork: Work closely with cross-functional groups including regulatory, medical affairs, and commercial teams to ensure project success.
• Regulatory and Medical Oversight: Offer guidance on regulatory preparations, monitor clinical trials, and ensure adherence to GCP standards.
• Data-Driven Problem Solving: Employ a creative mindset for operational challenges and prioritise critical work streams effectively.
  
  

Location and Travel

• Location: Boston, MA (Hybrid 2 -3 days on site)
• Travel: Anticipated travel is less than 10%
• Type: 12-month, part-time contract (25 - 30 hours per week)

If you are a motivated, experienced professional passionate about making an impact in the Oncology domain, we'd love to hear from you. Apply now to be part of this transformative opportunity with our client!

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

To find out more about Real, please visit www.realstaffing.com

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Part-time

Job function

• Job function

  Production, Quality Assurance, and Research

• Industries

  Pharmaceutical Manufacturing

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