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Career Openings


Sr. Director, Clinical Strategy & Communications

ID: 1541
Department: Medical Science Communications
Location: Cambridge Headquarters
# of Openings: 1

Description

Position description:

The Senior Director, Clinical Strategy & Communications will serve two critical roles: (1) key consultant to Clinical Affairs. Regulatory Affairs, PV, Clinical Operations and other areas for all questions related to IW-3718 development including protocol design, regulatory strategy, safety assessment and clinical trial design and execution; (2) key consultant and project contributor for scientific communication platform, publication strategy, scientific exchange, and Opinion Leader engagement related to IW-3718.  The Senior Director, Clinical Strategy & Communications reports to the Vice President, Medical Scientific Affairs, and is a part-time (20 hour per week) position

 

Responsibilities:

  • Serves as clinical and drug development Gastroenterology therapeutic subject matter expert within R&D, with particular focus on IW-3718 for persistent GERD

  • Works directly with MSA GI therapeutic area lead and lead study physician to coordinate activities that support IW-3718 development and scientific communications projects

  • Provides key input and contributes to development and execution of scientific communication platform, publication strategy, and scientific exchange strategy for IW-3718

  • Supports Gastroenterology MSLIW-3718 scientific exchange strategy and helps to develop scientific exchange materials and executes training as needed

  • Provides key consultation for clinical study design, protocol development and study execution by providing technical and strategic insights

  • Consults on IW-3718 regulatory strategy

 

Basic qualifications:

  • M.D., O.D., or equivalent;

  • 15 plus years’ pharmaceutical industry experience and at least 5 years’ experience in drug development with specific focus on GERD drug development (i.e. PPIs)

 

Preferred qualifications:

  • Established expertise in the development and implementation of medical scientific communications materials;

  • Extant relationships with GERD opinion leaders and history of positive collaborations

  • Demonstrated knowledge of clinical development and regulatory landscape relative to GERD treatments

  • Expertise in clinical research and development, and/or clinical/scientific consulting with experience as an investigator in clinical trials ideal

  • Demonstrated expertise in evaluation and analysis of clinical/scientific data, ideally with successful publications thereof.

  • Superb written communication skills.  Accomplished in creation of scientific exchange content, and/or scientific training materials.  Record of medical and/or scientific publications preferred;

  • Understanding of the legal and regulatory guidelines affecting the dissemination of medical information and product promotion;

  • Record of accomplishment of successful collaboration and relationship building, including experience working in co-marketing or co-development arrangements, is preferred;

  • Expertise in Good Publication Practices and other legal and regulatory guidelines affecting the communication and dissemination of medical and scientific data.


Ironwood 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 protected veteran status.





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