Clinical Scientist, Fsp - Support
By Fortrea At , Remote $100,000 - $145,000 a year
EBS/BA/MS/Ph.D. in Life Sciences with 2+ yrs relevant clinical research experience
Pharmaceutical and clinical drug development experience in a Clinical Scientist role
Proven ability to effectively manage multiple complex studies
2 years of Medical Monitoring experience required
Aggregate Data Review experience required
Excellent Excel and PP skills required
Senior Clinical Data Scientist
By Karius At , Remote $124,000 - $186,000 a year
5+ years experience, preferably at a diagnostic, biotech or pharmaceutical company analyzing large datasets, proficient in SQL, Python, R, or SAS.
Experience with data visualization, translating clinical data and information into a visual context to support publication and results reporting.
Excellent analytical skills to interpret complex clinical data, identify trends, and draw accurate conclusions.
Strong communication skills with the ability to communicate complex data analysis results to both technical and non-technical stakeholders.
Collect, organize, and interpret statistical information from clinical databases, coded data, and other specified data sets.
Conduct statistical modeling to support both internal and external research projects.
Clinical Biospecimen Scientist Jobs
By ICON At , Remote
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 Scientist Jobs
By Parexel At , Remote
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 Application Scientist Jobs
By CooperSurgical At , Remote $110,000 - $180,000 a year
Provide in-clinic biopsy support and training, ensuring product adoption is fully implemented in-house, with scientific “non-sales” skills
Run local workshops and training in collaboration with the Account Managers, senior CAS, Marketing and Medical Affairs
Participate in the global online training program offering by Medical Affairs
5+ years of Embryology experience required
Ensure that clinics consistently partner with CooperSurgical to drive (and demonstrate) best practices for clinical outcome
Bring back insights from clinic visits to Marketing to help the Commercial team identify opportunities for improved partnership with clinics
Senior Clinical Scientist Jobs
By Parexel At , Remote
Provides scientific input to Study Manager (SM) for data management activities (e.g., Electronic Data Capture, Data Review Plan, Case Report Forms)
Supports Study Management/Medical Writing activities as needed to achieve CTT deliverables
Minimum 2 years pharmaceutical experience with demonstrated leadership responsibilities required.
Reports to Parexel (PXL) assigned Line Manager with day-to-day direction from Client
Complete training assigned by Client and/or EP, as necessary, including general training requirements, SOPs, and system and process related training
BS/BA in Life Sciences with 7+ years clinical research experience
Clinical Scientist – Clinical Development (M/F/D) (Us)
By HOOKIPA Pharma Inc. At New York, NY, United States
Must have project management skills (develop short range plans that are realistic and effective)
Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming
PhD, MD, PharmD, or MS in life sciences with some previous experience in clinical research or clinical development experience.
Experience in working in an umbrella and/or basket clinical study design.
Proficient experience in medical writing such as authoring or co-authoring documents such as protocol, clinical study report, investigators brochure, patient narrative.
Experience in performing review of clinical trial data in order to identify trends in safety or efficacy data.
Clinical And Health - Scientist 1
By Niktor At Frederick, MD, United States

Essential Functions Demonstrate a basic understanding of scientific principles, biology Ability to perform routine tasks accurately and efficiently. Cell Culture and maintain cells using aseptic ...

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 Scientist Assistant Ii
By Vanderbilt University Medical Center At Nashville, TN, United States
The responsibilities listed are a general overview of the position and additional duties may be assigned.
Makes decisions and recommendations that have an impact on clinical research activities with minimal supervision from faculty
Formulates and conducts clinical research on problems of considerable scope and complexity
Provides clinical research expertise in an ongoing capacity
Independently interprets, organizes, executes, and coordinates clinical research assignments
Oversees the coordination of the Center’s journal club, works in progress meeting, guest lectures, and annual Alzheimer’s Disease Research Day
Senior Clinical Laboratory Scientist
By County of Contra Costa, California At , Martinez, 94553 $122,902 - $149,388 a year
Eager. Your willingness to learn new techniques and skills will be invaluable.
Knowledgeable. You will need to know clinical terminology, methods, and procedures.
2. Training and Experience Evaluation:
Organized. You will need to maintain accurate records.
Focused. There will be various work demands and it is important that each is prioritized.
Training in various specialty areas
Clinical Scientist - Immunology
By Merck Sharp & Dohme At , North Wales, 19454 $88,480 - $139,100 a year
Ability to manage multiple competing priorities with good planning, time management and prioritization skills
May be responsible for tracking study timelines using project management tools.
Working knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
Good understanding of the principles of project planning & project management
Supporting other scientists with imaging vendors, clinical outcome assessments, biomarker sample collection and management, and external data monitoring committee.
Building analytical skills to drive operational milestones
Remote: Clinical Scientist (2) (233682) Jobs
By Black Diamond Networks At United States

Job Description Client is looking to add Clinical Scientist consultants to the team for a 6+ month assignment. Must come with experience in the Neurovascular Medical Device space. 2-3 years is ...

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)
Senior Clinical Research Scientist
By ŌURA At Boston, MA, United States
Excellent project management skills, including the ability to prioritize tasks, manage timelines, and meet deadlines
Establish and manage research partnerships with academic organizations, healthcare institutions, commercial partners, and key opinion leaders to foster collaborative research initiatives
Ensure compliance with regulations, ethical guidelines, and data privacy requirements throughout the research process
Strong understanding of research design, methodologies, and regulatory requirements
Exceptional written and verbal communication skills, with the ability to effectively present complex scientific concepts to both technical and non-technical stakeholders
Experience in building, managing and/or mentoring a team of researchers is highly desirable