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Pharmaceutical Data Review Scientist Jobs

Data Review Auditor Jobs
By Catalent At , Greenville, 27834
Interpret data and make recommendations to management for improvement or potential concerns
Assist in complying with any other company and/or departmental objectives as directed by analytical management
Compare laboratory data against specifications and trend data where applicable to determine if results meet requirements
High school diploma or equivalent with at least 6 years of experience in a laboratory setting.
Associate degree in Biotechnology, Chemistry or equivalent science degree with 4 years of experience in a laboratory setting.
Bachelor’s degree in a science-related field (e.g. Biology, Chemistry, Pharmaceutical Sciences) with 3 years of experience in a laboratory setting.
Data Review Clerk Jobs
By Harris County Toll Road Authority At Houston, TX, United States
Previous clerical or data entry experience.
Ability to work under instructions from supervisors and managers
Strong written, oral communication and interpersonal skills
Strong analytical skills. Ability to reason and solve problems independently
Verifies transaction data from external parties agrees to system transactions.
Receipts, reconciles, and posts cash/monies to appropriate accounts; may perform wire transfers as required.
Entry Level Scientist - Data Review
By Eurofins Lancaster Laboratories At Columbia, MO, United States
Experience in a laboratory setting or GMP pharmaceutical setting.
Good organizational skills; ability to follow direction and good communication skills are required.
Strong computer, scientific, and organizational skills.
Not a coding or data science position*
Excellent communication (oral and written) and attention to detail.
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
Data Analyst, Pharmaceutical Jobs
By Randstad USA At Bedford, MA, United States
• Strong experience with appropriate programming tools such as Python required
• Self-starter with strong attention to detail and solid organizational skills required
• Basic knowledge of radioactive decay preferred
• Validate performance of the tool against published lists of isotopes
Data Review Scientist- Entry Level (Onsite)
By Eurofins Lancaster Laboratories At Lancaster, PA, United States
Verify scientific data is of sound quality following all method, industry, and client requirements where applicable.
Previous experience with LIMS preferred
Bachelor's degree in chemistry, mathematics, physics, or other related degree concentration, or equivalent directly-related experience
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Determine if data is compliant and defendable based on industry regulations and methodology.
Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
Entry Level Associate Scientist: Data Review
By Eurofins Lancaster Laboratories At Lancaster, PA, United States
Verify scientific data is of sound quality following all method, industry, and client requirements where applicable
1 year experience operating LC/MS, GC/MS, ICP/MS, ICP-OES, HPLC and/or GC or reviewing the data generated from them
Experience in a cGMP-compliant lab
Experience performing/reviewing method development and validation
Experience with extractables and leachable testing
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Data Review Associate Scientist: Extractables And Leachables
By Eurofins Lancaster Laboratories At Lancaster, PA, United States
Verify scientific data is of sound quality following all method, industry, and client requirements where applicable
1 year experience operating LC/MS, GC/MS, ICP/MS, ICP-OES, HPLC and/or GC or reviewing the data generated from them
Experience in a cGMP-compliant lab
Experience performing/reviewing method development and validation
Experience with extractables and leachable testing
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Pharmaceutical Data Analyst Jobs
By Insight Global At Philadelphia, PA, United States
• Support US REMS and ex-US Risk Management Program operational data and reporting requirements
Required Knowledge, Skills, and Abilities:
• Support for active monitoring of products that require risk management programs
• Categorize REMS and ex-US Risk Management Program required reports in the REMS Strategy & Operations dashboard
• Track and trend categories of REMS and ex-US Risk Management Program and vendor required reports
• Assist with reconciliation activities performed for US REMS and ex-US Risk Management Programs
Specialist, Bioassay, Data Review
By Moderna At Norwood, MA, United States
Previous experience reviewing data for GDP/GMP compliance as well as audit trail review
Previous experience managing quality records such as change controls, deviations, and lab investigations
Family care benefits, including subsidized back-up care options and on-demand tutoring
Generous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents
Moderna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
Here’s What You’ll Need (Minimum Qualifications)
Data Analyst - Pharmaceutical
By ZETTALOGIX INC At United States
• Knowledge of relational database concepts, proficiency with SQL, experience in R, SAS, or similar language
*Must have Pharmaceutical Industry experience
• Demonstrated experience working with various business intelligence and data visualization tools.
Visas: USC, GC, EAD-GC, H4-EAD, H1B
• Analyze promotional data to extract actionable insights using various analytics techniques.
• Develop and execute on promotional analytics measurement plans
Scientist I, Pharmaceutical Development
By Lupin Pharmaceuticals At Coral Springs, FL, United States
Strong English language skills including writing ability and oral communication.
Set up and operate formulation and testing instrument, and manufacturing and packaging process equipment. Conduct instrument and process troubleshooting.
Write protocols, methods, standard operation procedures, and contribute to submission documents independently. Design experimental studies and write reports with minimal supervision.
Design studies and conduct evaluation and selection of raw material (APIs, excipients, primary and secondary packaging material, device component material etc.).
Design process development studies and conduct evaluation and optimization of manufacturing and packaging process for orally inhaled products.
Qc Data Review Specialist
By Alcami Corporation At , Wilmington, Nc
Voluntary benefits including short & long-term disability, life, accident, critical illness insurances
· Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
· Excellent written and oral communication skills.
· Applies job skills and company policies and SOPs to complete a broad range of difficult tasks.
Competitive salary with career advancement opportunities
Medical, dental and vision coverage from day one
Senior Scientist Ii, Pharmaceutical Development, Cmc Biologics
By AbbVie At San Francisco Bay Area, United States
Lead AbbVie global drug product initiatives and manage direct reports.
Prior experience demonstrating independent critical thinking for technical problem-solving and driving fundamental science through innovative science is highly desirable.
Excellent communication and written skills are required.
Generate high-quality data based on sound scientific principles and prepare formulation data summaries, technical reports, scientific presentations, and regulatory documents.
Raise the external influence of Abbvie in the scientific community through external presentations, patent applications, and publications.
South San Francisco-based position with 10-20% business travel.
Pharmaceutical Scientist (Telework Eligible)
By FDA At Silver Spring, MD, United States
Natural Resources Management and Biological Sciences Series, AD-0401:
For more information, please see: OPM Occupational Series Qualification Requirements.
b. Outstanding candidates can be defined by existing outstanding work experience, outstanding performance rating, or both.
To be placed into a Cures position, candidates must meet the following criteria:
1. Scientific, Technical, and Professional Fields
2. Qualified and Outstanding Candidates
Clinical Lab Scientist Ii - Data Review (Remote)
By Myriad Genetics Inc. At , South San Francisco, 94080, Ca
Word processing and data management skills
Reviewing and interpreting patient call review in the laboratory information management system (LIMS) prior to test report release
Maintaining updated understanding and knowledge of the methods used in the laboratory
At least two years of experience working in a high-complexity molecular clinical laboratory as a licensed staff member (preferred)
One year of pertinent laboratory experience and/or training covering the specialties of the laboratory (required)
Prior experience with polymerase chain reaction (PCR)–based and/or next-generation sequencing (NGS) methods and data analysis (preferred)
Pharmaceutical Formulation Research Scientist
By SRI International At Menlo Park, CA, United States
Experience and in-depth knowledge in design, development and evaluation of parenteral formulations or tablet/capsule oral formulation development is desirable.
Experience in pharmaceutical industry is a plus but not required.
Excellent written and oral communication skills are required. An established publication record is a plus.
Evidence of good organizational skills and Evidence of attention to detail.
Contribute to projects to bring in new capabilities and drive efficiency for SRI’s Service Desk.
Due to government requirements candidates must be a US Citizen

Are you looking for an exciting opportunity to use your scientific expertise to review and analyze pharmaceutical data? We are seeking a Data Review Scientist to join our team and help us make a difference in the world of medicine. You will have the chance to work with cutting-edge technology and collaborate with a team of experienced professionals. If you are passionate about data and have a keen eye for detail, this could be the perfect job for you!

Overview A Pharmaceutical Data Review Scientist is responsible for reviewing and analyzing data from clinical trials and other sources to ensure accuracy and compliance with regulatory standards. They must be able to interpret and evaluate data to ensure that it meets the requirements of the regulatory agency. Detailed Job Description The Pharmaceutical Data Review Scientist is responsible for reviewing and analyzing data from clinical trials and other sources to ensure accuracy and compliance with regulatory standards. They must be able to interpret and evaluate data to ensure that it meets the requirements of the regulatory agency. The Data Review Scientist must be able to identify discrepancies and errors in the data and provide recommendations for corrective action. They must also be able to communicate effectively with other departments and stakeholders to ensure that data is accurate and up-to-date. Job Skills Required
• Strong analytical and problem-solving skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Knowledge of regulatory standards and guidelines
• Proficiency in data analysis software
• Ability to interpret and evaluate data
Job Qualifications
• Bachelor’s degree in a related field such as biology, chemistry, or biochemistry
• At least three years of experience in a related field
• Knowledge of Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP)
• Experience with data analysis software
Job Knowledge
• Knowledge of regulatory standards and guidelines
• Knowledge of Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP)
• Knowledge of data analysis software
Job Experience
• At least three years of experience in a related field
• Experience with data analysis software
Job Responsibilities
• Review and analyze data from clinical trials and other sources
• Identify discrepancies and errors in the data
• Provide recommendations for corrective action
• Communicate effectively with other departments and stakeholders
• Ensure that data is accurate and up-to-date
• Interpret and evaluate data to ensure that it meets the requirements of the regulatory agency