Kendra Bock

Background

About Kendra Bock

Mid-Senior Level, patient, adaptable, and highly motivated associate with 15+ years experience in the clinical research industry with a Contract Research Organization. Experience leading teams as a Safety Project Lead and Safety Workflow Manager. Additional positions included Senior Safety Specialist, Clinical Research Associate, and Project Team Assistant. Proficient in telecommuting with more than 12 years working remote. A hard worker and quick learner with a passion for science and commitment to life-long learning. I began my career in the pharmaceutical industry, while earning a Masters degree from Campbell University in Clinical Research, followed by two years as a traveling Clinical Research Associate. I then moved into safety compliance and have advanced my understanding and knowledge of clinical and post-marketing trials for twelve years. Extensive experience with clinical and post-marketing trials with drug indications such as Pneumonia, HIV, Breast Cancer, Prostate Cancer, Acne, Acute Bacterial Skin Infection, Overactive Bladder, Uterine Fibroids, Atrial Fibrillation, Hypertension, Transient Ischemic Attack, Cerebrovascular Accident, Chronic Obstructive Pulmonary Disease, Bronchitis, Constipation, Irritable Bowel Syndrome, Crohn's disease, Ulcerative Colitis, Chronic Pain, Chronic Migraines, Diabetes I, Diabetes II, Glaucoma, Ocular Hypertension, Dry Eye, Uveitis, Age-related Macular Degeneration, Major Depressive Disorder, and Aesthetics. I recently had an opportunity for professional growth and obtained a Master's degree in Business Administration, while living abroad in South Korea for my husband's job relocation. In Jun2023, we returned back to the states and I am very excited for the opportunity to join a company with a healthy, respectful, team-working climate and collaboration. I would love the opportunity to talk over projects that could use support and look forward to the chance to jump in on your team. Thank you for reviewing my profile.