Director, Clinical Development - King of Prussia, PA, United States - Joulé

Description

Clinical Development Medical Director

Location:
Must be local to King of Prussia, PA


Type:
Perm


Start Date:

ASAP
Oncology

Early Phase Development

Prefers someone who is not a contractor.

Clinical Development Medical Director

In collaboration with the clinical teams, the primary role is to lead and execute early/late-stage clinical trials for oncology products in development.

Participates in the design/planning of clinical studies and helps with the interpretation of study results. Establishes and approves scientific methods for design and implementation of clinical protocols, data collection systems and final reports. May recruit clinical investigators for research studies. Responsibilities also include adverse event reporting and safety responsibilities monitoring.

Design, prepare, and initiate study protocols and other required documentation in compliance with project plans, federal regulations, GCP, and good medical practice.

Act as medical monitor for company sponsored trials.

Support project teams with therapeutic area specific information.

Collaborate with internal safety group in analyzing and reporting of safety data from clinical trials.

Analyze and interpret other clinical trial data and prepare reports for regulatory agencies and publication.

Ensure consistency of scientific and development strategies for oncology products in development.

Maintain the highest level of scientific and clinical knowledge in relevant disease specific area.

May on case-by-case basis supervise employees, both directly and indirectly through a dotted line structure or via other subordinate supervisors.

MD (board certification or eligibility in Oncology or Hematology/Oncology desirable but not essential) required with a minimum of 8 years of post-residency experience.

Drug development experience in biotechnology or pharmaceutical industry, or a combination of academia and industry


Note:
Individuals with extensive academic experience but without experience in the pharmaceutical industry may be considered

Hands-on experience in the design, execution, and reporting of controlled clinical trials in oncology.

Participated in clinical oncology studies with molecular targeted or immunological therapies.

Understanding of basic science relevant to clinical oncology (biochemistry, immunology, molecular biology and/or genetics).

Uses broad expertise or unique knowledge and skills to contribute to development of company objectives and principles and to achieve goals in creative and effective ways.

Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors

Regularly interacts with executives and/or major customers.

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