Our team helps medical device and pharmaceutical product manufacturers bring innovative, compliant and highly effective products to market with world-class expertise and extensive, independent testing capabilities at accredited facilities in the UK and USA. 
 
Our experienced medical device and extractables and leachables (E&L) testing teams will provide advice, guidance and recommendations as well as delivering test data to help you demonstrate compliance to regulatory guidance or specifications set out by the FDA, EMA, MHRA, USP, ASTM and ISO.

Smithers also supports the pharmaceutical industry and the development of biologics and vaccines from discovery through phase IV, with expertise that includes bioassays and high sensitivity assays. Our scientists have expertise in large molecule bioanalysis assay development, validation, and sample analysis.

Industry: Medical Equipment Manufacturing
Company Size: 501-1,000 employees

Smithers - Medical Device Testing

Savvy Admin PROD

Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development. PDS works with customers to develop and validate new methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials currently in different phases of the FDA regulated drug approval process. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories.

**Role**

Smithers PDS is seeking a Study Coordinator I or II to join our team in Gaithersburg, MD. The job level will be commensurate with previously related experience. This role assists in performing study-related critical activities with supervision/oversight from the Project Manager and department management. Primary activities include:

- Study Coordinator I: (1) performing quality review of data tables, reports and all study supporting documentation for accuracy and adherence to SOPs, GLP guidelines, and established laboratory policies and (2) identifying issues and deviations that affect the quality of study-related data and communicating these to the Project Manager or appropriate department manager.

- Study Coordinator II: (1) Watson and Excel data retrieval, (2) QC of data tables and reports and all study supporting documentation, (3) identifying issues and deviations that affect the quality of study-related data and communicating these to the Project Manager or appropriate department manager, and (4) drafting study plans and reports as needed.

This position is classified as exempt and paid on a salary basis. Exempt employees typically work 40 hours or more to adequately perform their responsibilities. Extended work hours may be necessary to support the business in meeting client deliverable commitments. Position is generally eligible for a hybrid work schedule with at least three days on-site once all training requirements have been adequately met and proficient performance is consistently demonstrated.

The annualized salary range for a Study Coordinator I or II position is $50,000 - $65,000 or $60,000 - $75,000, respectively. Experience and qualifications will determine salary and job level. Smithers PDS offers a comprehensive health insurance package including a choice of 3 medical plans, dental insurance, vision insurance, 401K retirement plan and PTO.

**Primary Responsibilities**

- Study Coordinator I

-

- QC review data summary tables from Watson LIMS and various Excel spreadsheet formats.

- QC review report drafts and finalization.

- Organize and maintain project data so it can be submitted for audit or archive in a timely manner

- QC run folders and notebooks

- Conduct back archivist related activities

- Study Coordinator II

- Assist the Project Manager with meeting client deadlines. This requires a complete understanding of the status of each active project and the agreed upon project timelines and deliverables.

- Create data summary tables from Watson LIMS and various Excel spreadsheet formats.

- Assure that all study-related information is archived on date that the report is finalized.

- Assist the Project Manager in delivering , plans, and reports to clients.

- With input and supervision from the Project Manager, assist in drafting Analytical Plans and to support all phases of the business (Transfer, Validation and Sample Analysis) using Smithers or client specific templates.

- Conduct back archivist related activities

- Review run folders, notebooks and other study-related materials and document deviations from SOPs, regulations and/or client specifications.

- QC run folders and notebooks

- Assure that all run folders, data tables and reports move through the internal process including QAU in sufficient time to meet client timelines.

- Assure that all QC and QA findings are responded to in a timely fashion and are complete and accurate.

- Attend Client Conference calls and provide meeting minutes for client conference calls when required.

- Other duties as assigned.

**Additional Requirements**

- Knowledge of GLP.

- Ability to multi-task and participate in multiple studies concurrently.

- Ability to ensure high quality data while working under the pressure of strict deadlines.

- Overtime and weekend work as required.

- Work may require the use of PPE (personal protective equipment).

**Qualifications**

- Study Coordinator I

- Minimum of an associate degree in Biological Sciences or equivalent experience preferred.

- Prior experience reviewing data in detail and identifying errors.

- Experience in an analytical laboratory. GLP/GCP Immunochemistry environment is preferred but not required.

- Study Coordinator II

- Minimum of a Bachelor’s Degree in Biological Sciences or equivalent experience preferred.

- Minimum of 2 years in a direct laboratory bench role or study support role such as QC/QA at a GLP, GMP facility, at least 1 of which occurred in an analytical laboratory environment under GLP regulation.

- Immunochemistry experience is preferred.

- Functional knowledge of Watson LIMS is a plus.

- Extremely strong competence using Microsoft Word and Excel especially with various formatting features.

- Must be detail-oriented and well organized with exceptional written and oral communication skills.

- Must have sufficient scientific background to understand scientific concepts of ligand binding assays (biomarkers, PK, immunogenicity, and cell-based assays).

#PharmaJobs

Study Coordinator

BioSpace is the digital hub for life science news and jobs. We provide essential insights, opportunities and tools to connect innovative organizations and talented professionals who advance health and quality of life across the globe.

Industry: Internet News
Company Size: 11-50 employees

BioSpace

Ready to shape the future of science and global health? ATCC, a leading nonprofit biological resources and standards organization, is seeking a Scientist, Biomedical Genomics to work hybrid in Gaithersburg, MD.

The Scientist for Biomedical Genomics is responsible for contributing to the implementation and computational analysis of 'omics data and next-generation sequencing (NGS) projects. This role requires expertise in analyzing and interpreting large, complex datasets, alongside an understanding of genetic influences on health and disease, bridging data science and medicine. The Scientist will design, develop, and maintain a robust code base for the analysis of RNA-seq, transcriptomics, whole exome sequencing (WES), and whole genome sequencing (WGS) data—adopting or developing cutting-edge methodologies and pipelines as needed. Proficiency with diverse bioinformatics tools is essential to process, analyze, and interpret the vast volumes of genomics data generated. They will collaborate with interdepartmental cross-functional teams on new product development, services, or informatics projects, focusing on the design, development, and maintenance of code bases for RNA-seq, transcriptomics, WES, and WGS data analysis.

The Scientist for Biomedical Genomics will collaborate with interdepartmental cross-functional teams on new product development, services, or informatics projects, focusing on the design, development, and maintenance of code bases for RNA-seq, transcriptomics, WES, and WGS data analysis. They provide training and mentorship to biologists and peers for technologies and collaborative projects. The Scientist will use professional concepts and organizational policy and procedure to independently solve complex problems in imaginative and practical ways, utilizing various tools to process, analyze, and interpret high volumes of genomics data.

Join ATCC and be part of a team that supports the global scientific community with trusted, authenticated biological materials.

**Responsibilities**

**Scientific Research & Innovation**

- Design and conduct experimental studies to support scientific discovery.

- Initiate, direct, and execute research and development strategies.

- Evaluate feasibility of scientific concepts for problem-solving and innovation.

- Maintain scientific integrity and stay informed on advancements.

**Laboratory Operations & Data Management**

- Plan and execute lab research, troubleshoot technical issues, and manage DNA/RNA sequence databases.

- Record, analyze, and interpret study data.

- Translate experimental protocols into SOPs and analytical work plans.

**Communication, Collaboration & Strategic Support**

- Develop research documentation including reports, presentations, and publications.

- Disseminate findings to internal and external audiences.

- Support grant/contract proposals and internal R&D projects.

- Facilitate technology transfer across business units.

**Qualifications**

- PhD in Scientific Discipline or Engineering Equivalent and 2-5 years' experience or equivalent experience.

- Demonstrated expertise using command line to interact with Windows and Linux operating systems, including but not limited to Command Prompt, Powershell, Bash, or Zsh.

- Demonstrated experience with scripting languages, including but not limited to: Python, R, Perl, Ruby, Java.

- Demonstrated experience with biomedical genomics data science.

- Familiarity with cloud computing platforms like AWS or Google Cloud for bioinformatics applications.

- Ability to create various types of visualizations, including line plots, bar charts, histograms, scatter plots, and heat maps, to represent data trends, distributions, and correlations.

- Strong understanding of next-generation sequencing (NGS).

- A track record of understanding bioinformatics applications, libraries and custom scripts preferred.

- Familiarity with Linux high-performance computing environments preferred.

- Experience with machine learning techniques and their application to biological data preferred.

**Benefits**

The expected salary range for this position is $105,000 to $115,000 annually. Actual compensation will be determined based on experience and qualifications as well as internal equity and alignment with market data. In addition to base salary, this role may be eligible for additional incentive compensation including regular merit increases and the corporate bonus program.

**We Invest in You**

- Health & Wellness:

- Comprehensive medical coverage and company paid Life Insurance, Disability Insurance, AD&D, and paid parental leave

- Work life balance with Paid Holidays and PTO

- Fitness and cell phone subsidies, and additional benefits such as legal services, pet insurance and additional supplemental coverage.

- Employee Assistance Program offering around-the-clock counseling

- Financial security:

- 401(a) (6% employer contribution) and 403(b) (2% match) retirement plans

- Exceptional career advancement opportunities, recognition, and rewards

- Corporate bonus program

- Mission Focused:

- Non-profit organization supporting critical life science research

- We give scientists the tools they need to make discoveries that improve and save lives

- Contribute to community involvement and social responsibility

Join ATCC, where we fuel your success, well-being, and development. We're a mission-focused non-profit Equal Opportunity Employer, celebrating a century of supporting global public health. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. Shape the future of science with us.

Scientist, Biomedical Genomics

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