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| | Click here or scroll down to respond to this candidateCandidate's Name (Noza)Farmington, MIPHONE NUMBER AVAILABLEEMAIL AVAILABLEOBJECTIVEDedicated and accomplished Clinical Research Scientist with extensive experience managing pharmaceutical drug trials and a strong medical background. Seeking opportunities to contribute my expertise in clinical research and medical knowledge to advance healthcare and patient outcomes. LANGUAGES FOR MEDICAL COMMUNICATIONEnglish Russian Tajik UzbekSKILLS Clinical Research Management: Expertise in overseeing and managing clinical trials, ensuring compliance with regulatory requirements and study protocols. Patient Care and Diagnostics: Proficient in-patient interactions, history collection, physical examinations, and diagnostic evaluations. Clinical Research Coordination: Skilled in coordinating multi-site studies, including patient recruitment, informed consent, and data collection. Sample Collection and Handling: Experienced in sample collection, packaging, shipping, and managing investigational products. Medical Record Keeping: Accurate and organized in maintaining patient records and handling medical documentation. Pharmaceutical Drug Trials: Knowledgeable in managing and conducting pharmaceutical drug trials across various medical fields. Patient Education: Adept at educating patients about their conditions, treatments, and study participation. Data Management and Analysis: Proficient in data entry, management, and analysis using various databases and software. Pharmacy Operations: Background in pharmacy practices, including medication inventory management and regulatory compliance. Electronic Medical Record (EMR): Skilled in utilizing EMR systems for documentation and patient management. Healthcare Policy and Regulations: Understanding of healthcare policies, regulations, and standards impacting clinical research. Teaching and Mentorship: Experienced in training, mentoring, and inspiring students, and junior staff in clinical research settings. Multilingual Communication: Fluent in English, Russian, Tajik, and Uzbek, with the ability to bridge communication gaps in medical settings. Regulatory Compliance: Knowledge of Good Clinical Practice (GCP), Institutional Review Board(IRB) requirements, and other regulatory standards. Project Management: Strong project management skills, including planning, execution, and monitoring of research projects. Problem Solving: Effective in identifying and addressing issues that arise during research trials or patient care. Team Collaboration: Proven ability to work collaboratively with healthcare professionals, researchers, and patients.EXPERIENCEClinical Trial Consultant and Oakland University Lecturer, Rochester, MI Consultant and Special LecturerJuly 2023 Present Contract Clinical Trial Coordinator in cancer research. Address patient concerns and collect samples. Pack and distribute samples to labs. Interact with sponsors and research patient data. Compile lists of eligible patients for trials and follow up with them. Medical multilingual Translator. Volunteer for nonprofit organization. Serve as a subject matter authority, bridging theory and practical application. Infuse real-world relevance into the curriculum through firsthand experiences. Utilize unique teaching styles to enhance learning enjoyability and memorability. Inspire students' passion for the subject matter and guide them in academic and career pursuits. Connect students with potential internships, job opportunities, and industry insights. Revival Research Institute, Southfield, MIClinical Research ScientistDecember 2021 - December 2023 Managed over 20 pharmaceutical drug trial studies in pulmonology, cardiology, gastroenterology, general health, and gynecology, out of 150 nationwide. Trained and supervised clinical research coordinators, ensuring compliance with certification requirements. Oversaw patient screening outcomes, ensuring eligible patients were selected. Coordinated clinical research coordinators at multiple study sites and allocated resources effectively. Trained and mentored new hires in conducting Subject Feasibility Questionnaires and inclusion/exclusion analyses for pharmaceutical drug trials. Developed patient screening questionnaires tailored to study requirements, assisted in documenting physical examinations, and managed investigational products in collaboration with the Principal Investigator. Led pharmaceutical trials across multiple medical fields, emphasizing adaptability and bridging the gap between patients and physicians. Continuously updated medical knowledge and fostered leadership in clinical science. Detroit Medical Center (DMC), Detroit, MISenior Clinical ExternAugust 2020 - September 2021 Collaborated with medical professionals in the outpatient cardiology clinic. Assisted in gathering patients' medical histories and observing physical examinations. Evaluated diagnostic findings and presented patients to attending physicians. Proposed treatment plans and engaged in discussions about alternative management approaches. Maintained patient records and contributed to a grant proposal for Transthyretin Amyloid Cardiomyopathy (ATTR-CM). Year-long hands-on volunteer experience during COVID-19, providing valuable care through direct patient interactions and collaboration with healthcare professionals. University of Michigan, Ann Arbor, MIClinical Research Coordinator HealthSeptember 2018 - April 2020 Managed the Pelvic Organ Prolapse study, screening potential participants and obtaining informed consent. Coordinated MRI visits, provided support during pelvic exams, and processed MRI films and images. Addressed volunteers' inquiries, arranged visits, and managed questionnaire distribution. Conducted chart reviews, data extraction, and database management. CVS Pharmacy, Farmington Hills, MIPharmacy TechnicianJune 2016 - November 2018 Supported patients and healthcare providers by assisting pharmacists. Ensured compliance with procedures and regulations. Collected patient and insurance information and addressed inquiries. Managed medication inventory and maintained drug and inventory logs. INTERNATIONAL EXPERIENCESamarkand Republic University, Samarkand, Uzbekistan Obstetrician and GynecologistJune 2007 - June 2008 Provided comprehensive patient care and management, including OB and gynecological surgeries, breast disorder oversight, women's health risk assessments, and labor and delivery attendance. Managed intrapartum complications and conditions like pelvic organ prolapse and urinary incontinence. Offered preventive medicine services and patient education on cancer screenings, contraception, and STIs. Conducted adnexal mass evaluations and cervical cancer screenings and participated in gynecologic surgeries. Gained research experience in post-term pregnancy over three years. Highlighted the importance of human connection and adaptability in healthcare, shaping a resilient, adaptable physician dedicated to compassionate patient care. EDUCATIONSamarkand State Medical Institute, UzbekistanMedical DoctorAugust 1997 - June 2004Samarkand Republic University, UzbekistanMD, OBGYNAugust 2004 - June 2007 |