Data Review Molecular Scientist Jobs

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.

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.

Knowledge of data structure, capture, analysis and visualization is desired; experience with Spotfire or Tableau would be beneficial.

Excellent organizational and interpersonal skills.

Excellent written and verbal communication skills.

Skills with working in research teams at interfaces and in multi-disciplinary environments is beneficial.

Non-standard Work Schedule, Travel Or Environment Requirements

Closely collaborate with Research partners to evaluate molecular attributes relevant to drug delivery and influence team strategies.

Prepare reports, publications and present to cross-functional teams and senior management.

Support some lab management duties as needed and assigned.

5+ years of academic and / or industry experience

3+ years of academic and / or industry experience

Experience in cardiovascular or muscle biology, working with stem cells, iPSC-derived cells or primary cells are strongly desirable.

Strong experience with cellular and molecular biology methodologies including cytotoxicity assays, gene expression analysis, RNAi technologies, immunocytochemistry is greatly preferable.

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.

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.

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

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

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)

Experience, Education and Specialized Knowledge and Skills

Contribute to research strategies across Exploratory and Discovery programs, applying expert knowledge of principles, theories, and concepts in areas of expertise.

Manage pharmacology work streams across functions internally and with CROs and academic labs externally.

Manage pharmacology research in a matrixed environment, as well as external academic collaborations and an extensive network of CROs.

Maintain knowledge of state-of-the-art principles and theories and apply this knowledge to the design, execution, and interpretation of experiments.

Experience translating cellular neurobiology to in vitro pharmacology assays.

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

Primary Job Duties and Responsibilities:

Acquires thorough technical and theoretical knowledge of research project and objectives during one to five (1-5) year post-doctoral appointment.

Experience in recombinant protein expression, drug-screening, and X-ray crystallography.

Experience in X-ray crystallography is required.

Experience in biophysical techniques including SPR and MST is preferred.

Knowledge of safety standards and maintenance of specialized equipment.

Broad knowledge of cheminformatics, bioinformatics, and QSAR methods and experience with the development of related data analysis pipelines and visualizations

Experience in working in multidisciplinary teams and working environment(s)

Excellent written and oral communication skills

Drug discovery experience in the field of biologics within industry or academics (industry preferred)

Experience with protein modelling software programs such as Rosetta, Schrodinger and/or MOE is considered a plus

Experience working with cloud compute services such as AWS S3, EC2 or Azure

Responsibilities also include analytical equipment procurement/qualifications, preparation and maintenance of SOP’s, determination, and control of critical reagents for example.

Collaborate with clinical operations and sample management to define sample journey and develop appropriate laboratory manuals.

Knowledge of GcLP requirements and understanding of current industry trends and regulatory expectations associated with analytical science.

Experience with RNA, biologics and cell therapy preferred

Experience in RT-PCR, ddPCR, NGS sequencing and other methodologies for clinical assays and basic validation principles

Working knowledge of the translational literature and competitive landscape in the RNA therapeutic field.

Manages research project with other institutions and investigators.

Several years of experience in writing or editing professional/scientific correspondence in a research environment.

Can “project manage” the process of assembling and directing stakeholders to meet deadlines.

Can work independently and manage and prioritize multiple tasks accordingly.

For policies, detailed benefits, and eligibility, please visit: https://hr.wustl.edu/benefits/

Collaborates with the PI on the design, conduct and reporting of research projects.

Maintain expertise through continuing education

Comply with applicable federal, state, and local regulations, health and safety policies and procedures, and the requirements of accrediting organizations.

Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements

Minimum 1 year of clinical laboratory testing experience is required

Previous experience performing molecular techniques, such as DNA extraction, PCR, sequencing, NGS, genotyping is preferred

Prior experience with sequence analysis and familiarity with sequence analysis software is a plus

Required Knowledge, Skills And Abilities

Accurately and efficiently complete data entry into Microsoft Office programs to maintain CCS databases.

Strong computer skills, ability to use basic office equipment.

Must have excellent customer service skills, exhibiting courteous, compassionate, and respectful treatment of internal and external customers at all times.

Previous laboratory or scientific research experience required.

Medical, dental and vision benefits

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)

Applies considerable scientific knowledge and experience in advancing the aims of the project.

Provides highly specialized skills, knowledge and/or expertise that is essential to the success of the project.

Plans, organizes, coordinates, directs and participates in scientific research projects.

Presents findings and writes articles for publication.

Supervises the design, development or adapting of equipment used in experiments or research to obtain desired results.

Develops innovative new approaches and/or new technology.