Job Overview: Collaborate with a team to support clinical development through study design, protocol writing, compliance monitoring, and data analysis for regulatory submissions in a dynamic research setting.
Primary Job Responsibilities:
Collaborate with experts to build the scientific basis for clinical trial designs.
Draft study-related documents, leveraging internal and external insights.
Contribute to Investigational Brochures (IBs) updates and regulatory responses.
Monitor study data for safety and compliance, and engage in complex data analysis.
Primary Job Requirements:Masters, PhD, or PharmD in a relevant field.
Demonstrated expertise within a clinical environment in both allergy and immunology
About Stratacuity:
Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member. We build lasting relationships with exceptional biopharmaceutical talent and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a Stratacuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.
PROVEN SCIENTIFIC PLACEMENT™
Stratacuity is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Stratacuity will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact us.