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Clinical Affairs Scientist Jobs

Clinical Scientist Jobs
By Parexel At Durham, NC, United States
Reports to Parexel FSP assigned Line Manager with day-to-day direction from the Client
Complete training assigned by Client and/or EP, as necessary, including general training requirements, SOPs, and system and process related training
BS/BA/MS/PhD in Life Sciences with 2+ years relevant career experience
If no degree in Life Sciences, must have significant experience in clinical development (>5 years)
Demonstrated oral and written communication skills
Excel and PowerPoint (PP) experience required
Clinical Affairs Scientist Jobs
By MDC Associates, Inc. At Beverly, MA, United States
Knowledge of applicable protocol requirements as provided in company training
Study sites and clinical study management
Provide input on content of submission documents based on experience, regulations and guidance available from regulatory bodies
Bachelor's degree in a health care or other scientific discipline or educational equivalent
5-10 years’ experience in a clinical environment or medical devices industry, with specific experience in in vitro diagnostic devices
Knowledge of the European Commission Medical and In Vitro Diagnostic Device Regulations.
Clinical Affairs Scientist- Clinical Development
By Agilent Technologies At San Francisco, CA, United States
Manages and oversees the governance, for internal and external stakeholders (Agilent and external laboratory sties, respectively).
4+ years of experience of industry experience in the fields of diagnostic, medical device and/or pharmaceutical products.
Knowledge of clinical study design, biostatistics, and Good Clinical Practice.
Experience working with external partners and/or regulatory bodies including the FDA.
Knowledge in oncology, companion diagnostic development, pathology, immunohistochemistry and/or next generation sequencing preferred.
Responsibilities include but are not limited to:
Associate Director, Clinical Scientist
By AbbVie At Lake County, IL, United States
Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols
Collaborate cross-functionally to help create a scientific platform in support of the regulatory, commercial and medical education strategy for late-stage assets.
Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.
Must possess excellent oral and written English communication skills.
Responsible for providing focused scientific and clinical study support from start-up clinical study report (CSR).
Contribute to creation of electronic database, IRT, and associated training documents and review data completeness and fidelity throughout study conduct.
Clinical Scientist Jobs
By Kelly At Philadelphia, PA, United States
Pharmaceutical and/or clinical drug development experience beneficial but not required
2 years medical monitoring experience preferred
Demonstrated oral and written communication skills
Excel and PP experience required
BS/BA/MS/PhD with 2+ yrs relevant career experience
Minimum FTE Years of Experience
Scientist, Clinical Jobs
By Revlon At , Edison, 08818, Nj
Effectively manages change in order to deliver business objectives.
Effectively prioritizes and manages complex projects / tasks
Manages key vendor partner relationships and work streams.
Minimum Education Required: Bachelor of Science in Biology, Life Sciences or Chemistry
Minimum Years Experience Required: 8-10 years
Excellent written & verbal communication skills (able to communicate to all levels within the organization)
Scientist, Clinical Jobs
By Revlon At Edison, NJ, United States
Effectively manages change in order to deliver business objectives.
Effectively prioritizes and manages complex projects / tasks
Manages key vendor partner relationships and work streams.
Minimum Education Required: Bachelor of Science in Biology, Life Sciences or Chemistry
Minimum Years Experience Required: 8-10 years
Excellent written & verbal communication skills (able to communicate to all levels within the organization)
Clinical Scientist Jobs
By Charlton Morris At New York, NY, United States
Maintain full understanding of clinical protocol, including mentoring of more junior employees on requirements.
At least 5 years of experience in clinical development (5+ Associate Director, 8+ Director level).
Demonstrated experience creating clinical trial protocols and regulatory documentation.
Excellent communication skills (written, oral and presentation).
Proficient knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile).
Senior/Clinical Scientist (based on experience)
Clinical Data Scientist Jobs
By Ontada At United States
2+ years of experience in SAS and advanced SQL skills
Must have 4+ years of work experience in clinical data analysis
Experience in mining Claims and EMR data, preferably oncology related data
Foundational Experience in any cloud platform (ability to perform data analysis and build data transformation logic)
Strong interpersonal, oral and written communication skills
Healthcare consulting and oncology experience
Clinical Scientist Consultant Jobs
By Palleon Pharmaceuticals At California, United States
Perform ongoing clinical data review and critical analysis of study data, partnering with clinical development and data management.
Strong knowledge of FDA/global regulatory requirements, ICH regulations, and GCP.
Experience in oncology drug development and/or immune-oncology clinical trials required.
Excellent communication and interpersonal skills.
Proven scientific writing skills for clinical/regulatory documents, and ability to evaluate, interpret and summarize complex data.
· Experienced clinical scientist with proven track record in solid tumor early clinical development.
Clinical Affairs Jobs
By ProKatchers LLC At West Sacramento, CA, United States

The Clinical Affairs Scientist I will support the Clinical Affairs team during Microbiology antimicrobial susceptibility testing (AST) clinical trials. The incumbent performs testing as defined ...

Clinical Scientist Jobs
By LanceSoft, Inc. At West Sacramento, CA, United States
Bachelor's degree in a Life Science or related field with 5+ years’ experience in laboratory experience.
Strong communication skills with the ability to work in a multidisciplinary team environment.
The Clinical Affairs Scientist I will support the Clinical Affairs team during Microbiology antimicrobial susceptibility testing (AST) clinical trials.
Assist with the coordination of clinical study materials including the receipt, ordering, distribution, tracking, and shipment to clinical sites.
Updating project lead(s) with data and any issues will be required, as well as an ability to work in cross-functional teams.
Familiarity with Excel and Data Analysis is desired.
Scientist - Scientific Clinical
By Procter & Gamble At Mason, OH, United States

Hand-on-techniques gained in academic or industrial settings.

A P&G Scientist Will Be Responsible For

Senior Clinical Affairs Specialist (Remote - Usa)
By Bionano At United States
Support input from clinical studies to development teams for key requirements and sample management.
Effective communication, organization, and time management skills.
Summary, Primary Duties, Skills And Experience
Manage project portfolio across clinical sites in multiple clinical studies.
Manage the publication process for internal publications including writing text and gathering data/figures from other contributors.
Experience working with technical teams.
Senior Clinical Lc/Ms Scientist
By Kelly At Kansas City Metropolitan Area, United States
Stay current with the latest developments in LC/MS technology, regulatory requirements, and industry trends.
Minimum of 3-5 years of experience in LC/MS-based assay development and validation
Hands-on experience with LC/MS instrumentation and software, including mass spectrometers, HPLC systems, and data processing tools.
Understanding of regulatory requirements for LDTs, including CLIA, CAP, and ISO guidelines.
Process-driven approach to development with strong analytical and problem-solving skills, with attention to detail and accuracy.
Excellent verbal and written communication skills, with the ability to collaborate effectively with interdisciplinary teams.
Clinical Scientist Jobs
By Bristol Myers Squibb At Princeton, NJ, United States

If BMS Careers Site link is not copy and pasting correctly, please add manually using the following address https //careers.bms.com/working-with-us

Uniquely Interesting Work, Life-changing Careers

Clinical Scientist-Associate Director Jobs
By Adaptimmune At Philadelphia, PA, United States
7+ years of industry-sponsored clinical trial management experience required. Experience with biologics or cell and gene therapy is a plus.
Prior experience with clinical protocol development and/or regulatory submissions and management
Proactive stakeholder management and communication of progress and issues
Strong knowledge of clinical operations and the regulatory process - experience independently running/managing multiple clinical trials preferably within the oncology area
EDC including trial management, data review, issuing and resolving queries, CRF design/review/ approval.
Lead the cross-functional Study Conduct Team – drive operational delivery and facilitate issue resolution.
Clinical Biospecimen Scientist Jobs
By ICON Strategic Solutions At United States
Experienced in collaborating with EDO/vendor management on oversight of all labs and with internal stakeholders to understand biospecimen strategy.
Laboratory or Clinical Research professional with at least 3 years of sample collection experience
Create study specific sample collection tables and ensure alignment with blood volumes needed versus allowed.
Graduate with a Bachelor of Science degree
Able to work East Coast hours, attend global meetings and occasionally travel internationally for team meetings
Key member of a study team to ensure biospecimens are collected, analyzed and data transferred as per the clinical protocol.
Clinical Data Scientist Jobs
By Loyola Medicine At Maywood, IL, United States
Proficiency in statistical software such as R or SAS, and database management.
3+ years of previous job-related experience.
EPIC certification or training minimum in Cognito, Clarity and Caboodle Data models.
Strong SQL and coding experience.
Programming skills in Python and R preferred.
Certification reimbursement (up to 1 certification)
Project Coordinator, Clinical Innovation, And State Gov Affairs
By AHIP At Washington, DC, United States
Maintains department records and manages supported executives’ deadlines and coordinates work with appropriate department staff.
Tracks and manages relevant committee lists on an ongoing basis.
Tracks and manages progress on relevant project plans.
This position has no supervisory responsibilities.
Advanced skills in Microsoft Office products (Outlook, WORD, Excel, PowerPoint, or similar graphic program),
The ability and willingness to master other software packages/computer skills in database manipulation.