Browse Average Salary Ranges for Biotechnology Jobs

Evaluates, develops, and maintains clinical database and analyzes clinical data. Codes, tests and documents databases. Performs data validation and develops algorithms for data management, typically using SAS programming language. May require a bachelor's degree. Typically reports to a supervisor or manager. Gains exposure to some of the complex tasks within the job function. Occasionally directed... View job details

Participates in the design, administration, and execution of clinical research trials. Conducts standard tests in accordance with established policies and procedures. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and... View job details

Participates in the design, administration, and execution of clinical research trials. Conducts standard tests in accordance with established policies and procedures. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and... View job details

Participates in the design, administration, and execution of clinical research trials. Conducts standard tests in accordance with established policies and procedures. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and... View job details

Participates in the design, administration, and execution of clinical research trials. Conducts standard tests in accordance with established policies and procedures. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and... View job details

Conducts statistical studies to generate data and insights used to innovate, plan and support improved healthcare outcomes and processes. Prepares analysis plans to ensure the best statistical methods are developed and utilized. Writes specifications for files, consistency checks, tables, and calculations used to collect and analyzes data from a variety of sources. Interprets analyses and prepares... View job details

Conducts statistical studies to generate data and insights used to innovate, plan and support improved healthcare outcomes and processes. Prepares analysis plans to ensure the best statistical methods are developed and utilized. Writes specifications for files, consistency checks, tables, and calculations used to collect and analyzes data from a variety of sources. Interprets analyses and prepares... View job details

Develops, writes, and edits medical content for various projects and initiatives. Conducts thorough research and gathers information from various sources to develop accurate and comprehensive medical documents, such as clinical study reports, protocols, and/or regulatory submissions. Reviews and interprets scientific and clinical data to effectively communicate complex medical information to diffe... View job details

Develops, writes, and edits medical content for various projects and initiatives. Conducts thorough research and gathers information from various sources to develop accurate and comprehensive medical documents, such as clinical study reports, protocols, and/or regulatory submissions. Reviews and interprets scientific and clinical data to effectively communicate complex medical information to diffe... View job details

Participates in the design, administration, and execution of clinical research trials. Conducts standard tests in accordance with established policies and procedures. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and... View job details