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
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 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
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 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 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

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 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 Biospecimen Scientist Jobs
By IQVIA At Durham, NC, United States

Job Purpose: Responsible for the implementation and end-to-end operational execution of each GCO clinical trial strategy as it relates to all biospecimens collected, including safety, ...

Biospecimen Coordinator - Irvine
By City of Hope At Irvine, CA, United States
Works under the supervision of the Manager Investigators, Disease Team Leads, and the direction of the Clinical Research Nurse.
Manages and orders all supplies required to obtain biospecimens.
Performs protocol-specific duties required per the research protocol, including but not limited to:
Confirms the presence of a signed informed consent from a subject prior to specimen collection.
Monitors clinic and other schedules to ensure subjects have been scheduled for upcoming protocol procedures which require research specimen collection.
Regularly performs an inventory to identify and discard expired collection tubes, etc.
Clinical Scientist Jobs
By Randstad Life Sciences US 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
Required Skill 1: Oncology clinical trial experience in the hematologic malignancies therapeutic area in the pharmaceutical industry
Required Skill 5: Strong knowledge of multiple myeloma.
Required Skill 4: Excellent written and verbal communication skills, detail-oriented organization skills, and team collaboration skills.
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.