Website Aldeyra Therapeautics, Inc.

Company Summary:
Aldeyra Therapeutics is a biotechnology company devoted to developing and commercializing next-generation medicines to improve the lives of patients with immune-mediated diseases. Aldeyra’s lead investigational drug product candidates are potential first-in-class treatments in development for dry eye disease, allergic conjunctivitis, and proliferative vitreoretinopathy. The company is also developing other product candidates for retinal and systemic inflammatory diseases.

Position Summary:
The scientist in this role will assist project teams to design, execute, and interpret pharmacology studies to facilitate the proof-of-concept of novel ideas, and eventual translation to the clinic.

Responsibilities include:
• Contract, manage, analyze, interpret, and report on in vitro and in vivo pharmacology studies for small molecule drug candidates.
• Identify and select CROs to conduct in vitro and in vivo pharmacology studies.
• Design studies; review and revise study protocols.
• Manage and serve as study monitor on studies.
• Ensure studies are conducted as designed.
• Troubleshoot problems with studies.
• Ensure appropriate contract documents are in place with CROs.
• Work with CRO to develop study protocols.
• Interpret study data.
• Review and revise study reports.
• Write study reports and addenda, as needed.
• Present study results to team and senior management.

Education/Qualification/Requirements
• Strong in vivo pharmacology background to inform CRO management
• Ph.D. in Pharmacology or closely related field
• 4 to 8 years of experience in biotech/small companies conducting and managing pharmacology studies. Must have extensive experience designing, executing, and interpreting in vivo pharmacology studies.
• Experience identifying, selecting, and managing contract laboratories.
• Experience with small molecules.
• Broad therapeutic area experience, including experience in immunology and ocular
disease.
• Experience working cross-functionally and on drug discovery/development project teams.
• Experience drafting pharmacology sections of INDs and/or other regulatory documents is a plus.
• Experience with academic and industry collaborations.
• Excellent written and verbal communication skills.
• Ability to manage multiple projects simultaneously.
• Budget, cost, and time management skills.
• Expertise with MS Office and statistical analysis programs.
Leadership and Communication: Excellent written and verbal communicator with the ability to facilitate/articulate recommendations and key decision points to senior management; demonstrated experience reducing complex subjects to key points; ability to develop a strong network across company.
Relationship Management: Ability to develop new business relationships and to nurture partnerships with internal and external stakeholders. Ability to provide strong cross-functional team leadership to maintain alignment and to set and meet collaborative operational goals.

To Apply:
Please email your cover letter and resume to info@aldeyra.com or to send a resume via an alternative method, please mail it to our corporate address:

Aldeyra Therapeutics, Inc.
Attention: Human Resources
131 Hartwell Avenue
Suite 320
Lexington, MA 02421

To apply for this job email your details to info@aldeyra.com