Clinical Research Coordinator with PharmD Training

SANJEEDA AMREEN SHEIK

**********@*******.*** Novi, MI 248-***-****

Permanent U.S. Resident – No Sponsorship Required

LinkedIn: linkedin.com/in/dr-sanjeeda-amreen-s-9b5508346 OBJECTIVE

Clinical Research Coordinator with international clinical trial experience and PharmD training. Strong background in regulatory documentation, patient screening, adverse event reporting, and ICH-GCP compliance. Currently gaining U.S. healthcare system experience as a Pharmacy Technician while transitioning into U.S. based clinical research operations. PROFESSIONAL EXPERIENCE

Pharmacy Technician, Canton, MI December 2025 – Present Walgreens

Responsibilities:

Provided direct patient interaction and patient support by addressing medication- related questions, ensuring clear understanding of dosage, usage, and safety instructions.

Maintained accurate data entry and electronic documentation in pharmacy management systems, including EPIC HER system, supporting patient safety and workflow efficiency.

Ensured compliance with federal and state healthcare regulations, maintaining accurate documentation and patient records in accordance with HIPAA guidelines.

Reviewed prescriptions for accuracy, drug interactions, contraindications, and dosage safety.

Processed insurance claims and prior authorizations, supporting coordination between patients, providers, and payers.

Assisted patients with medication counseling under pharmacist supervision.

Maintained controlled substance logs and performed inventory management with strict regulatory compliance.

Collaborated with physicians and healthcare providers to clarify prescriptions and therapy adjustments.

Supported medication safety initiatives and error-prevention protocols. Clinical Research Coordinator March 2023 – May 2025 NOMAD LIFE SCIENCES (ADAM INFOTECH)

Responsibilities:

Supported patient care by interacting with patients, monitoring vital signs, and assisting in specimen collection and laboratory procedures while ensuring accurate documentation and adherence to safety protocols.

Pre-screen and screen potential participants; schedule and prepare for consent and enrollment processes.

Prepare participant visits, verify protocol procedures, and provide visit support.

Monitored vital signs and reported abnormalities to healthcare teams.

Enter data into electronic systems, handle source documentation, and help resolve data queries.

Observe protocol compliance, report adverse events or deviations, and help with the maintenance of audit-ready files.

Coordinate communications among investigators, participants, labs, and external monitors or sponsors.

Keep accurate and up-to-date records such as screening logs, enrollment records, and regulatory documents.

Maintained accurate patient records and clinical documentation.

Provided direct patient interaction and patient support by addressing medication- related questions, ensuring clear understanding of dosage, usage, and safety instructions.

Help prepare IRB submissions, consent forms, and binders of regulatory documents under close supervision.

Internship Trainee

Maharaja’s Institute Of Medical Sciences, INDIA April 2022 – October 2022 Responsibilities:

Interacted with patients to collect medical history and assist in clinical assessments.

Provided clear instructions and support to patients during visits, ensuring comfort and understanding.

Communicated patient concerns to healthcare teams to support timely and effective care.

Measured and recorded vital signs including blood pressure, heart rate, temperature, and respiratory rate.

Provide patient education through supervised counseling on proper use of medications, potential side effects, and lifestyle modification to promote adherence to treatment.

Work closely with healthcare practitioners, including physicians and nurses, to exchange information about drug treatments and help with patient treatment plans.

Help to maintain compliance with pharmacy regulations and statutes, such as record- keeping and maintenance of controlled substances.

Assist in identifying search for and notify adverse drug reactions, search for drug interactions, and other drug issues.

Participate in clinical rounds, educational workshops, and training programs to be updated with respect to pharmaceutical practices and innovations. Project Intern

King George Hospital, INDIA October 2021 – March 2022 Responsibilities:

Assist in collecting and reporting accurately COVID-19 vaccination and other conditions ADRs via stated databases and set protocols.

Assist in tracking ADR frequency, intensity, and trends; aid in data analysis to identify patterns and potential safety concerns.

Participate in follow-up contact (calls or survey) with patients or doctors to capture additional ADR data and allow for prompt case closure.

Conduct literature review to understand safety profiles of COVID-19 vaccines from clinical trials and post-marketing surveillance data.

Assist preparation of summaries of safety and submission documents to regulatory authorities or internal safety committees.

Assist development and dissemination of educational materials for ADR awareness and reporting procedures to patients and healthcare professionals. EDUCATION

Doctor of Pharmacy (PharmD)

JNTU Kakinada - Avanthi College of Pharmaceutical Science. Graduated: October 2022

Relevant Coursework: Clinical Research Methods, Pharmacology, Medical Terminology, Epidemiology, Biostatistics.

CERTIFICATIONS

Diploma in Clinical Research - 2023

ICH-GCP Certification – 2025

Drug Safety Certification – 2025

Regulatory Affairs Certification – 2025

Clinical Data Management Certification - 2025

SKILLS

Clinical Trial Monitoring.

Vital signs monitoring/laboratory procedures

Site Management & Regulatory Compliance.

Data Collection & Integrity Management.

Regulatory Documentation Management (FDA, ICH, GCP).

Patient Recruitment & Informed Consent.

Adverse Event Reporting (AE/SAE)

Effective Communication & Stakeholder Collaboration.

Strong Organizational & Time Management Skills.

TECHNICAL SKILLS

EPIC EHR

Software: MEDRA, Oracle Clinical,

SharePoint, MS Office Suite (Outlook, Word, Excel, PowerPoint, OneNote), Windows. ADDITIONAL INFORMATION

Languages: English, Hindi, Telugu

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