ClinicalResearchAssociate

**Use Your Power for Purpose** Our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy. **What You Will Achieve** In this role, you will: * Coordinate and support all activities related to clinical trials, assisting managers in their execution. * Assist in site activation activities, including gathering necessary documentation. * Review data for quality and completeness, ensuring timely submission to data management and supporting patient safety and eligibility. * Coordinate with sites to finalize budget worksheets and contractual agreements, maintaining accurate site-level information on the clinical trials registry. * Support the study team with regulatory submissions, maintain the Electronic Library and Records Archive, and attend investigator meetings as required. **Here Is What You Need**(Minimum Requirements) * BA/BS with at least 2 years of experience or MBA/MS with any years of experience * Demonstrated success in prior roles, including within matrix organizations * Deep understanding of quality and regulatory requirements across various countries * Knowledge of International Conference on Harmonization Good Clinical Practices and local regulations * Proficiency in applications used in clinical trials * SOP compliance knowledge and expertise on all relevant SOPs * Effective verbal and written communication skills, and fluency in English **Bonus Points If You Have**(Preferred Requirements) * A Master's degree combined with relevant therapeutic area experience * High level of project management skills * Strong analytical and problem-solving skills * Ability to w