[Hiring] Director, Clinical Science @Lantheus

Role Description

The Director, Clinical Science will be responsible for the design and interpretation of Lantheus clinical studies, including protocol development and oversight. This position has a key role in clinical development and supports progression of the investigational product from IND through registration. The position will operate in a cross-functional matrix environment and work with multiple functional groups. The successful candidate will have wide-ranging responsibilities and the ability to work within a highly collaborative, dynamic, and interdisciplinary team. This is a remote position open to applicants authorized to work for any employer within the United States.

Essential Functions

• Responsible for the relevance and accuracy of clinical development planning and guidance for a clinical study.
• Contribute to authoring and lead design/reviews of key product and study-related documents and deliverables, including but not limited to:
  • Clinical Protocols and amendments
  • Investigator Brochures
  • Study Manuals
  • Case Report Forms
  • Informed Consent Forms
  • Clinical Study Reports
  • Annual Reports
  • Regulatory submissions
  • Abstracts and publications
• Responsible for the oversight of clinical study execution as clinical lead in close collaboration with Clinical Operations and internal/external stakeholders.
• Works with investigative sites and/or study teams to answer protocol-related questions and resolve study conduct issues.
• Reviews clinical data listings, patient profiles, and summaries to ensure data collection, interpretation, and reporting is consistent with the protocol and company processes.
• Prepare and may present protocol designs, clinical data, and other information at advisory boards, investigator meetings, and site initiations.
• Works closely with internal and external stakeholders to accumulate scientific and clinical knowledge necessary to support clinical development execution.
• Supports regulatory interactions and the development of clinical sections for regulatory correspondence and submissions.
• Participates in review and management of safety reports and submissions.
• Participate in clinical and safety database reconciliation.
• Supports project team with conduct of clinical studies, including clinical trials registration and results reporting.
• Interacts with internal and external stakeholders in support of clinical trial objectives and deliverables.
• Leads preparation of advisory board meetings and KOL interactions; leads development of clinical publications.
• Works with external experts to develop abstracts, manuscripts, and study design presentations.
• Works in a strategic and facilitative role by leveraging clinical development expertise.
• Serves as clinical representative on product development team.
• Leads drug development team across a complex, matrixed environment.
• Attends scientific meetings to remain abreast of clinical developments.
• Actively promotes safety rules and awareness.

Qualifications

• Advanced Degree preferred (e.g. MD, PhD, or PharmD).
• 7 - 10 years of relevant experience in pharmaceutical industry in clinical development preferred.
• Oncology and/or Radiopharmaceutical clinical development experience preferred.
• Clinical development experience across all phases of development (I - III).
• Proven track record of working with investigators, site staff, external experts, Contract Research Organizations, and vendors.
• In-depth knowledge of regulatory guidelines and ICH/GCP.
• Experience in developing and writing study protocols, clinical study reports, and other study documents.
• Excellent verbal and written communication skills with ability to work across functions in a multifunctional matrix environment.

Requirements

• Approximately 25% routine overnight travel based on business need.

Core Values

• Let people be their best.
• Respect one another and act as one.
• Learn, adapt, and win.
• Know someone’s health is in our hands.
• Own the solution and make it happen.

Benefits

• Comprehensive health benefits package including medical, prescription drug, dental, and vision coverage.
• Life and disability benefits.
• Pre-tax accounts.
• 401(k) with company contribution.
• Generous time off package including paid vacation, holidays, sick days, and paid parental leave.

Salary Information

The pay range for this position is between $191,000 and $286,000 annually. Actual base pay offered may vary depending on a number of factors such as job-related knowledge, skills, and experience.

Application Information

Interested candidates can apply at Lantheus.com. Applications for this position will be accepted until July 30, 2026.

Equal Employment Opportunity

Lantheus is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's actual or perceived characteristics.

Contact Information

Any applicant requiring an accommodation in connection with the hiring process should make a request to the Lantheus Talent Acquisition team at [email protected].

E-Verify Employer

Lantheus is an E-Verify Employer.