CAREER LIBRARY
Pharmaceutical Industry
Learn more about the Pharmaceutical industry, read our articles and explore the job roles.
Read the latest articles on Pharmaceutical, and learn more about the industry.
Job Roles in Pharmaceutical
Pharmaceutical companies develop and produce medications and drugs.
An Analytical Chemist is responsible for studying the chemical composition of substances and developing analytical techniques for quality control, process improvement, and compliance with safety regulations.
Specializes in designing, implementing, and monitoring clinical trials involving animals to assess drug efficacy and safety before they are considered for human use.
A Bioanalytical Chemist performs complex chemical analyses on biological samples to support research and development in medical, pharmaceutical, and environmental fields.
A Clinical Data Manager is responsible for collecting, coordinating, and analyzing data from clinical trials to ensure accuracy and regulatory compliance. They closely work with research teams in the biomedical field.
A clinical pharmacologist specializes in understanding the effects of pharmaceutical drugs on humans, including drug composition, chemical properties, and the appropriate use of medications in medical treatment.
A Clinical Project Manager oversees the management of clinical trials in the medical field, ensuring that projects adhere to regulatory standards, timelines, and budgets.
A Clinical QA Auditor is responsible for ensuring that clinical trials and other research activities comply with relevant regulations and standards, and that data integrity is preserved.
A Clinical Research Associate is responsible for monitoring clinical trial progress, ensuring compliance with regulatory standards, overseeing study sites, and assuring the integrity of data collected.
A Clinical Research Scientist is involved in conducting research and trials to test the efficacy and safety of new medical treatments, drugs, and interventions.
A Clinical Study Designer is responsible for creating and developing protocols for clinical trials in the pharmaceutical or biotechnology fields.
A Clinical Trial Manager oversees the administration and progress of clinical trials, ensuring adherence to regulatory requirements and protocols, and manages the clinical operations team.
A Clinical Trials Manager oversees the administration and execution of clinical trials, ensuring compliance with regulatory requirements, protocol adherence, and coordination of research activities.
A Drug Approval Specialist works on evaluating and analyzing data from clinical trials to ensure that pharmaceutical drugs meet regulatory standards for safety and efficacy before they can be marketed to the public.
A Drug Discovery Scientist is involved in the early stages of pharmaceutical development, conducting research to identify and create new medications.
A Drug Safety Associate is responsible for monitoring and reporting the effectiveness and any adverse effects or side effects of pharmaceuticals and drugs in the market.
A professional responsible for monitoring and reporting on the safety of pharmaceutical products, including adverse event reporting and ensuring compliance with regulatory requirements.
A Formulation Scientist develops and tests new product formulations in a lab, often for pharmaceuticals, cosmetics, or food products, ensuring stability and regulatory compliance.
This role involves leading and overseeing the development of regulatory strategies for products globally, ensuring compliance with all applicable laws and guidelines within the pharmaceutical, biotechnology, or health-related industries.
A GMP Auditor is responsible for examining and ensuring compliance with Good Manufacturing Practices within production facilities, often related to pharmaceuticals, food, or medical devices.
A Medical Science Liaison acts as a scientific and clinical expert connecting pharmaceutical and healthcare companies with healthcare professionals. They educate and inform on new research and medical products.
A Medical Writer creates scientific documents that detail research findings, product use, and other medical information. They primarily work for pharmaceutical companies, healthcare agencies, or medical publishers.
A Medical Writing Specialist researches and writes scientific documents related to pharmaceuticals, medical devices, and clinical evaluation reports.
A scientist responsible for developing, validating, and implementing methodologies for experimental and analytical procedures, often in pharmaceuticals or biotechnology.
A Pharmaceutical Affairs Specialist oversees the regulatory compliance of pharmaceutical products, ensures adherence to health policies, and manages submissions for drug approval processes.
A Pharmaceutical Buyer is responsible for purchasing medications and medical supplies for pharmacies, hospitals, or medical facilities, ensuring stock levels meet demand.
A Pharmaceutical Compliance Officer ensures that a pharmaceutical company adheres to regulatory requirements and internal policies, focusing on legal compliance and ethical standards within the industry.
A professional responsible for planning and executing marketing strategies to promote pharmaceutical products and services to healthcare providers and consumers.
A pharmaceutical product manager is responsible for overseeing the development, marketing, and sale of pharmaceutical drugs. They work to ensure products are compliant with regulations and meet market demands.
This role involves managing projects within the pharmaceutical industry, including drug development, clinical trials, regulatory approval processes, and product launches.
A pharmaceutical researcher is involved in the scientific study, experimentation, and development of drugs and medications for medical use, aiming to improve health outcomes.
This role involves managing sales teams and strategies for selling prescription drugs and medical products to healthcare providers and facilities.
A pharmaceutical scientist conducts research, experiments, and trials to develop new drugs and medical treatments, ensuring safety and regulatory compliance.
A pharmacoeconomics analyst evaluates the economic impact of pharmaceutical products, examining cost-effectiveness, value, and outcomes related to medications and health interventions.
A professional responsible for the sales and promotion of pharmacogenomic products and services, which involve the study of how genes affect individual response to drugs.
A healthcare professional who analyzes genetic information to predict drug response and tailor medications to the genetic makeup of individual patients.
A pharmacologist is a scientist who studies the actions and effects of drugs on biological systems. They are critical in the development of new medicines.
A Pharmacology Research Scientist is involved in the study of the effects of drugs on biological systems, and the development of new drugs for medical use.
A Pharmacovigilance Associate is responsible for monitoring and reporting the effectiveness and any adverse effects or side effects of pharmaceutical products post-market to ensure drug safety and compliance with regulations.
A pharmacovigilance officer is responsible for monitoring the safety of pharmaceutical products, detecting and assessing adverse events, and ensuring compliance with drug safety regulations.
A Regulatory Affairs Analyst is responsible for ensuring that a company's products comply with regulations and standards. They assess and analyze regulatory policies and coordinate with agencies.
A Regulatory Affairs Associate is responsible for ensuring that products meet all of the regulatory standards and requirements set by government bodies before they can be marketed or sold.
A Regulatory Affairs Consultant advises companies on the legal and regulatory aspects of product development and marketing, ensuring compliance with applicable laws and guidelines.
A professional responsible for ensuring that an organization complies with all of the regulations and laws pertaining to their business. They work with federal, state, and local regulatory bodies to keep up-to-date with the regulations.
Responsible for ensuring that an organization complies with all of the regulations and laws pertaining to their business. Works with federal, state, and local regulatory bodies.
A Regulatory Affairs Manager is responsible for ensuring that a company's products comply with all regulations and laws pertaining to their industry. They handle regulatory submissions and communicate with regulatory agencies.
This role involves managing projects within an organization to ensure that products comply with all regulations and laws pertinent to the industry. The manager liaises with regulatory agencies and prepares submissions for market authorization.
This job involves ensuring that an organization complies with all of the regulations and laws pertaining to its business. They work with federal, state, and local regulatory agencies and personnel on specific issues affecting their business.
A Regulatory Scientist ensures products meet regulatory standards. They compile and analyze scientific data, handle regulatory submissions, and communicate with regulatory agencies for approvals in sectors like pharmaceuticals, biotechnology, and food.
A Regulatory Specialist ensures that a company's products and procedures meet all regulations and laws pertaining to their industry. They handle regulatory submissions and compliance.
A Stability Coordinator typically oversees the storage and testing of products or materials to ensure they remain stable over time. They are responsible for monitoring the conditions in which products are stored and ensuring that they meet quality and safety standards.
A Synthetic Chemist specializes in creating and studying new compounds through various chemical synthesis processes, often for applications such as new drug development or material innovation. The role requires a deep understanding of organic and inorganic chemistry principles.
A toxicologist is a scientist who studies the effects of chemicals, substances, and exposures on humans, animals, and the environment. They assess risks and conduct research to ensure safety.
A Toxicology Manager oversees the analysis of the toxic effects of chemicals and substances on humans, animals, and the environment, ensuring safety and compliance with regulations.
A Toxicology Specialist assesses the impact of chemicals, materials, and products on human health and the environment, conducting experiments and risk assessments.
A professional specialized in researching and developing medications and treatments specifically for animal health and veterinary medicine.