Clinical Research Medical Writing
Resume:
FAHMEEDA FURQAN SYED
MEDICAL WRITING
***********@*****.***
S K I L L S
P R O F I L E
MBBS-qualified medical professional with over 5 years of clinical experience in hospital and outpatient settings, currently undergoing training in pharmacovigilance and clinical research. Strong foundation in medical terminology, diagnosis, and patient care, with a growing expertise in regulatory guidelines and drug safety documentation. Detail-oriented and skilled in medical communication, literature review, and translating complex scientific information into clear, structured content. Seeking to leverage medical expertise and analytical skills in a medical writing internship within a clinical or regulatory setting.
E D U C A T I O N
DECCAN COLLEGE OF
MEDICAL SCIENCES,INDIA
MBBS
2006-2011
C O U R S E S /
C E R T I F I C A T I O N S
L A N G U A G E S
English
Urdu
Hindi
s k o i e, i l l i n o i s
CRA certification course
(ongoing)
Master pharma Regulatory affairs:
FDA/EMA global(ongoing)
Medical writing for healthcare
professionals (ongoing)
Pharmacovigilance
training(completed)
MEDICAL AND SCIENTIFIC KNOWLEDGE
Over 5 years of clinical experience in hospital and outpatient care Deep understanding of human anatomy, physiology, pathology, and pharmacology
Familiar with adverse drug reactions, medical conditions, and ICD-10 classification
Strong grasp of medical terminology and treatment protocols MEDICAL WRITING & COMMUNICATION
Skilled in scientific literature review and summarization Experience writing patient records, discharge summaries, and case reports Ability to convey complex medical content clearly for varied audiences Structured writing with attention to grammar, tone, and accuracy PHARMACOVIGILANCE & CLINICAL RESEARCH (IN TRAINING) Knowledge of ICH-GCP guidelines and clinical research processes Understanding of adverse event reporting and drug safety documentation Exposure to protocol writing, informed consent forms (ICFs), and case report forms (CRFs)
Familiarity with MedDRA/WHO-ART coding and regulatory documentation
(based on training content)
TECHNICAL TOOLS
Proficient in MS Word, Excel, PowerPoint
Reference management tools: Mendeley, Zotero
Literature research using PubMed, Cochrane Library Basic knowledge of EDC systems (if applicable from training) SOFT SKILLS
Strong written and verbal communication
Attention to detail and quality assurance
Analytical thinking and data interpretation
Time management and ability to meet tight deadlines Adaptability and eagerness to learn in new domains July 2019 - July2023
Apollo Life, Occupational Health Centre, Novartis, Hyderabad Medical Officer
Responsibilities and duties at work include:
• Provide Primary Care Services as follows–Urgent medical and nursing services including
resuscitation, stabilization and assessment and diagnosis, treatment and referral as necessary
• Assess the urgency and severity of presenting problems through history taking, examination and
investigation
• Recommending and, where appropriate, referring for appropriate interventions and procedures,
including but not limited to prescribing, counselling, psychological interventions, advising and
education
• Referral for diagnostic, therapeutic and support services as required
• Provide timely clinical and culturally appropriate health services through – Ongoing health and
development assessment and advice
• Provide and administer annual vaccinations for preventative care
• Interventions to assist people to reduce or change risky and harmful lifestyle behavior
• Improve patient health through – Health education, counselling and information provision about
how to improve health and prevent disease and interventions or treatments that treat risk factors.
• Patient Management - Ensure patient information in patient register is correct and up to date for
reporting purpose
• Participation in clinical audit as required by clinical or administrative indication WORK EXPERIENCE
• Jan 2019 - July 2019
M. S. Polyclinic and Diagnostic Centre
Family Physician
Responsibilities included but not limited to – providing Maternity Services, pre-natal and post-nata
care; provide routine care and general examination of patients; Advise diagnostic tests such as CB
X-ray, Ultra-sound and necessary lab work; provide first-aid and emergency care to accident patient
acute care management, vaccinate patients including adults and infants; Referring patients to
specialist consultants and hospitals as required.
October 2012 - July 2014
Care Hospital, Nampally, Hyderabad
Resident Doctor
Worked for general surgery, internal medicine,cardiology as well as other departments and I. C. U
Performed the following duties at the hospital:
• Admitting patients to wards, taking history, providing Initial assessments, examining general
condition, order necessary investigations like lab tests, X-ray, etc., and diagnosis
Provide primary patient care and report the condition of the patient to Specialist Doctors and
Consultants
• Assist and participate in minor OT procedures
• Performing first-aid such as dressings, catheterizations, prescribing alternate drugs and deciding
upon the need of Intensive Care for patients
• Provide aid in resuscitating patients while on duty in ICU
• Taking consents for Surgeries, procedures, shifting to ICU and AMCU
• Document the details like writing death Certificates, incident reports, Doctor’s proforma, notes and daily treatment charts August 2023-march2025
Romark L.C. Tampa FL – Clinical Clerkship Assistant
• Develop, send, collect, review, and process clinical trial-related documents (i.e., informed consent forms,
FDA forms, curriculum vitae, financial disclosure forms, etc.) in compliance with requirements set forth by regulatory agencies (e.g., FDA, EMEA, ICHGCP, SOPs, and working practice guidelines, etc.)
• Maintain tracking tools and spreadsheets of required investigative site essential documents and contact
information.
• Assist with the preparation of study amendments, laboratory manuals, and other clinical trial-related
documents as assigned.
• Maintain and coordinate the generation of clinical trial status reports and tracking spreadsheets and/or
databases.
• Generated and reviewed management reports from internal tracking systems at requested intervals.
• Participate in cross-functional internal study team meetings and take minutes as requested.
• Will take direction and instruction from the Lead Clinical Trial Specialist.
• Carrying out periodic Inspection and Audit as per SOPs.
• Conducting the audit of Vendor/Third-party service providers.
• Managed projects including e-CRF writing, protocol reviewing, manuscript development, blog posts,
patient education material, newsletters, and medical website content
Contact this candidate