Ayesha

Ayesha

$15/hr
Clinical Research, Data entry, Sales, Marketing, Content writing.
Reply rate:
-
Availability:
Full-time (40 hrs/wk)
Location:
Istanbul, Istanbul, Turkey
Experience:
6 years
AYESHA ANUM- Istanbul, Turkey https://www.linkedin.com/in/ayesha-anum/ WORK EXPERIENCE NOV 2022 – CURRENT Lund, Sweden (Remote) CLINICAL RESEARCH ASSOCIATE II (FREELANCE) DIGNITANA AB    Working on ongoing Oncology medical device clinical trials. Manage and Extract Data for the purpose of Publication. Ensure the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, Regulations and SOP’s. JUL 2022 – JULY 2023 California, United States (Remote) CLINICAL TRIAL PROJECT MANAGER OCULAR IMAGING RESEARCH AND READING CENTRE (OIRRC) · Experience in Ophthalmology and Neurology related clinical trials. · Work with CROs/Sponsors in managing, storage, QC and Grading of related data. · Assist team in designing, developing, testing and improving of trial management and data capture system for clinical trial management. · Support clinical science team in development of trial protocol, ICFs, CRFs and other study related documents. · Communicate with developers’ team regularly and on daily basis. · Ensure that the studies are conducted in compliance with the Protocols, Regulations and SOPs · Maintain trial master file and ensure updated versions of all trial related essential documents. · Facilitate site management activities, site initiation, monitoring and site training. · Covers Clinical Trial Geographical sites in Asia, Europe and USA · I am an integral part of the team dedicated to enhancing the company’s workflow efficiency. NOV 2021 – DEC 2021 Istanbul, Turkey INTERNATIONAL MEDICAL ADVISOR GLOBAL TURKEY CLINIC · · · Assess Patients needs and present suitable treatment method. Coordinate and communicate with doctors about case studies in Plastic surgery and Hair Transplant. Used CRM software to organize leads and daily tasks. MAR 2018 – AUG 2021 Karachi, Pakistan CLINICAL RESEARCH ASSOCIATE II MUSAVVIR STEM CELLS CLINIC • • • • • Develop and outline trial protocol, establish trial sites, train staff and trial materials. Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects. Ensuring compliance with SOPs, Local regulations and ICH-GCP. Complete on site and remote monitoring activities in compliance with ICH-GCP. Develop study procedures, methodology and instructions for clinical trials staff, as well as design data collection tools. Strive to continuously maintain a thorough and current understanding of pertinent regulations, guidelines and best practices in clinical research. Data collection, Monitoring, designing trial materials, Designing Feasibility and Eligibility questionnaires. Site selection and Activation, maintain TMF. • • • DEC 2016 – DEC 2017 Karachi, Pakistan CLINICAL RESEARCH ASSISTANT DR. RUBINA GHANI MOLECULAR & PATHOLOGICAL LABORATORIES • • • • Research assistant in different laboratory procedures. Collect and analyze data for research purposes. Write and contribute to publications. Assist in Regenerative medicine and Stem cells therapy for Muscular Dystrophy, Congenital disease, Diabetic foot, Hair and skin diseases. • Perform routine chemistry SEP 2018 – DEC 2018 Karachi, Pakistan CLINICAL LABORATORY INTERN CITY HEALTH CARE • • Perform different lab tests Lab data collection and interpretation EDUCATION AND TRAINING 2014 – 2019 PHARM-D DOW UNIVERSITY OF HEALTH SCIENCES Field of study Pharmacology and Therapeutics, Pharmaceutics, Pharmaceutical Organic Chemistry Final grade CGPA: 3.5 Thesis Assessing Clinical Drug Dose Adjustment in Renal Impaired Patients on The Basis of Serum Creatinine Levels. DEC 2019 – DEC 2020 United Kingdom ACUTE MEDICINE NHS UK JUL 2011 – AUG 2013 PRE-MEDICAL Sir Syed Govt. Girls College 2000 – 2011 MATRICULATION St. Lawrence’s Convent Girls School LANGUAGE SKILLS Mother tongue(s): ENGLISH | U R D U Other language(s): TURKISH B2 | KOREAN B1 | CHINESE A2 | FRENCH A2 ADDITIONAL INFORMATION COURSES AND CERTIFICATIONS           Certified Clinical Researcher (IPPCR) National Institute of Health US. Certified investigator and site personnel Good Clinical Practice GCP-ICH Genesis Research Services. . Certified Good Clinical Practice NIDA Clinical Trials Network. Certified Good Clinical Practice from London School of Hygiene and Tropical Medicine. Certified Antibiotic Guardian by Public Health England, NHS Scotland. Regulatory Updates for Clinical Research Professionals SOCRA. Certified Good Clinical Practice from Society of Behavioral Medicine. International Vaccinology course from Vaccinology Institute. Examination of Corona Virus COVID-19 St. George University. Pharmacotherapy: Current and future horizons IVPN-Network HIPAA, GDPR, Kevin Mitnick Security Awareness Training. AVAREF WHO Clinical Trials. UNIVERSITY OF MANCHESTER (CPPE) · · · Consultation skills in pharmacy Neurology Early recognition of sepsis JACKSON LABORATORY USA COURSES · · · · · Identifying Red Flags in Cancer and its risks (University of Connecticut School of Medicine). Identifying and Managing Lynch Syndrome (University Of Connecticut) Precision medicine: Pre Natal-Cell Free DNA Screening (Accreditation from American Medical Association) Precision medicine: Genomic Testing for the Healthy Individual (AAMS) Precision medicine: Genetic Testing in Pediatric Neurology (AAMS). THE GLOBAL HEALTH NETWORK · · · Certified ICH-GCP E6 Certified Good Clinical Laboratory Practice Data Management for Clinical Research Studies WORLD HEALTH ORGANIZATION (WHO) COURSES · · · · · Critical care Severe Acute Respiratory Infection Training course. Poliomyelitis Management and its Eradication. Antimicrobial Stewardship: Competency Based Approach for Clinicians Competency Based Learning AVAREF WHO Clinical Trials. CONFERENCES AND SEMINARS Attended Seminar on Emerging Antibiotics Resistance, MDR and XDR. Attended 5th ICon online webinar GCED Sponsored by APCEIU and UNESCO in Seoul, South Korea HONOURS AND AWARDS Merit based HEC scholarship. – Higher Education Commission of Pakistan (HEC) awarded throughout undergraduate period based on good academic record. RESEARCH WORK AND PUBLICATIONS  Final year Thesis on Assessing Clinical Drug Dose Adjustment in Renal Impaired Patients on The Basis of Serum Creatinine Levels.  Presented Research Paper on Therapeutic Weapon Against Cancer Use of Olive Oil at DUHS DICE Health Expo 2016 & 8th Annual Research Day in Dow University of Health Sciences, 2017.  Presented Research Paper on Rapid Detection & Genotyping of MTB by Gene Flow Hybridization & PCR at ICEHSR 7th international conference on endorsing health science research by Advance Educational Institute and Research Centre (AEIRC).  Workshop Facilitator and Research Assistant in Stem Cells Therapeutics in 12th Biennial International Conference on Microbiology held in Abbottabad University of Science and Technology.  Published Research paper in Turkish Journal of Hematology & Pakistan Journal of Medicine and Dentistry on Evaluation of NESTROFT in Screening & Diagnosis of Beta Thalassemia Trait in Pakistani Population VOUNTEERING EXPERIENCES: UN Volunteer (Active) Youth Unity Welfare Organization (Active) Truth Community (Active) Recovery Alliance (Active) SKILLS:          Develop and maintain patient tracking tools; communicate status to investigators, management and relevant departments.   Exceptional organizational skills, attention to detail, a strong work ethic, and experience administratively managing clinical trial contracts.          Strong attention to details, and ability to adhere to project deadlines. Accurate, detail oriented; handles multiple tasks         Maintain IRB regulatory material at the local site level. Coordinate adverse event/serious adverse event submissions to the IRB and sponsors.   Clinical project management for multiple multicenter clinical trials.          Data management, preparation of study documents, study protocols, case report forms, study progress reports and clinical site communication                   Function independently in a clinical research setting, provide time flexibility for scheduling the study visits.   Strong skill in using Microsoft applications including Word, Excel, PowerPoint, and Outlook, as well as research databases, electronic case report forms, and other computer based programs.
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