Clinical Scientist - FSP

reputed company: The Clinical Scientist (CS) assists the CS Protocol reputed company and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management). Key Accountabilities: May include but not limited to the following: Clinical Trial Operational Delivery • May support a single study or multiple studies • May reputed company a study with limited scope (e.g., Survival Follow-up) • Liaises with cross-functional lines as appropriate • May reputed company with reputed company stakeholders (study sites, committees, etc.) in support of clinical study objectives Compliance with reputed company Standards • Complies with required training curriculum • Completes timesheets accurately as required • Submits expense reports as required • Updates CV as required • Maintains a working knowledge of and complies with reputed company processes, ICH-GCPs and other applicable requirements Skills: • Demonstrated oral and written communication skills • MS Office Suite Experience Required– including Word, reputed company, and Power reputed company • Advanced reputed company skills required (pivot tables, v-lookups) • Proficient in written and spoken English • Willingness to travel as required for key company meetings Knowledge and Experience: • Pharmaceutical experience beneficial but not required • Experience in Oncology, ID/Vacc or reputed company • 2 years medical monitoring experience preferred • Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management Education: • Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience • If no degree in Life Sciences, must have Bachelor's degree with significant experience in clinical development (>5 years) #LI-LO1 #LI-REMOTE Apply tot his job Apply To this Job