Verified recordBiotechnology Research

Seema Mule

Regulatory Affairs Intern at Biotecnika

Based in Malmo, Sweden

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Seniority

Staff

Department

Science

Location

Malmo

Industry

Biotechnology Research

Company size

369

Contact information

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Email

1 credit

s•••••••@biotecnika.org

Phone

5 credits

+46 ••• •••• ••••

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Background

About Seema Mule

Dynamic and adaptable Healthcare Professional with over a decade of experience in Healthcare Consulting, now transitioning into Clinical Research and Pharmaceutical roles. Recently completed specialized education in Clinical Research, Pharmacovigilance, and Clinical Data Management to align with global standards. Recognized by the Swedish Higher Education Authority (UHR) for possessing qualifications equivalent to a Master's degree in Healthcare and Hospital Administration. Hardworking and committed to excellence, I bring a strong willpower and deep interest in life sciences, ensuring quality output for the global population. Proven expertise in healthcare quality assurance, clinical research, patient care, and holistic counseling. Adept at navigating cross-cultural work environments with a focus on compliance, quality assurance, and data integrity. Core Competencies: Healthcare Quality Assurance & Control: Internal Audits, NABH Accreditation, Infection Control Clinical Research & Data Management: Clinical Trial Management Systems (CTMS), Adverse Event Reporting Pharmacovigilance: Signal Detection, Risk Management, CIOMS, PSUR, DSUR Regulatory Affairs: GxP Compliance, FDA Regulatory Submissions, SOP Development Healthcare Administration: Patient Care, Holistic Counseling, Process Optimization Cross-Cultural Adaptability: Effective communication and collaboration in diverse teams Career Objective: To secure a position within clinical research, pharmacovigilance, regulatory affairs, quality control, quality assurance, clinical data management, or regulatory compliance in the pharmaceutical or healthcare industry. My goal is to leverage my extensive healthcare expertise, advanced certifications, and cross-cultural skills to enhance quality standards, compliance, and data integrity, contributing effectively to the global healthcare and pharmaceutical sectors. Driven by dedication and passion for life sciences, I strive to deliver quality outcomes that benefit large populations around the world.

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