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Preclinical Study Manager Jobs

Home Study Case Manager
By Rising Ground, Inc At , Yonkers, 10705 $61,400 a year
Bachelor of Social Work (BSW) degree or an equivalent degree in education, psychology, sociology, or other behavioral science.
Two years’ experience working with youth in the social service field.
Knowledge of child welfare and immigration related legislation
Excellent verbal, written communication and organizational skills are essential
Responsible for completing Home Studies assigned by the HS Supervisor meeting ORR expected timeframe.
Maintain ongoing consultation with the HS Supervisor of any obstacle or barrier to timely completion of the HS report.
Study Manager - Immunology
By Merck Sharp & Dohme At , North Wales, 19454, Pa $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 trial leads with imaging vendors, clinical outcome assessments, biomarker sample collection and management, and external data monitoring committee.
Building analytical skills to drive operational milestones
Study Manager - Oncology
By Kelly At Philadelphia, PA, United States
May be responsible for tracking study timelines and will be proficient in project management tools
Pharmaceutical and/or clinical drug development experience beneficial but not required
Demonstrated oral and written communication skills
Excel and PP experience required
BS/BA/MS/PhD with 2+ yrs clinical research experience
Minimum FTE Years of Experience
Senior Global Study Manager
By Seven Life Sciences At United States
Minimum of 7 years of clinical trial management experience in oncology or biotech/pharmaceutical industries
Oversee study conduct, including site initiation, monitoring, close-out, and management of external vendors
Participate in the selection and management of Contract Research Organizations (CROs), including contract negotiation and performance evaluation
Knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials in the EU and US
Develop and manage study timelines, budgets, and resource plans for global clinical trials in the EU and US
Collaborate with the Medical Director to ensure clinical trial data is accurate, complete, and consistent with regulatory requirements and study protocol
Study Abroad Program Manager
By Barnard College At New York, NY, United States
Help to prepare financial and risk-management trainings for Barnard faculty leading programs abroad.
In-depth knowledge of international education, in particular study abroad programming for US students
Significant international experience and demonstrated cross-cultural communication skills
Manage the summer study abroad application cycle; ensure that programs are active and available for applications; review and approve student applications.
Manage the student application process through the Terra Dotta platform, support faculty in accessing the system and making admissions decisions.
Experience developing and running institutional faculty-led programs
Study Abroad Program Manager
By Barnard College At New York City Metropolitan Area, United States
Help to prepare financial and risk-management trainings for Barnard faculty leading programs abroad.
In-depth knowledge of international education, in particular study abroad programming for US students
Significant international experience and demonstrated cross-cultural communication skills
Manage the summer study abroad application cycle; ensure that programs are active and available for applications; review and approve student applications.
Manage the student application process through the Terra Dotta platform, support faculty in accessing the system and making admissions decisions.
Experience developing and running institutional faculty-led programs
Local Study Manager Jobs
By Sanofi At Bridgewater, NJ, United States
Certification level of Project Management (PMP/PMI)
Accounts for the set-up, completion, and adaptations of project management tools at country level (CTMS, Control room…)
Be the main link to the local monitoring team in the management of studies
Align on joint KOL/investigator management
Proficiency in complex trial management
Manage and maintain Country Study Budget during course of study
Preclinical Project Manager Jobs
By REVA Medical, LLC. At San Diego, CA, United States

Summary Of Essential Duties And Responsibilities

Study Director Jobs
By Eurofins Lancaster Laboratories At South Brunswick, NJ, United States
Responsibilities as stated in GLP regulations.
Hands-on working knowledge of the tests that will be under their responsibility.
Good administrative skills and leadership ability. Must communicate effectively and write well.
Assist in protocol development, design and implementation.
Data interpretation and report writing.
Overall, day-to-day laboratory operation including supervision of technical staff assigned to your studies.
Program Manager, Study Operations
By Verily At Raleigh, NC, United States
Experience in study project management and prior management of contracted resources/CROs.
8+ years of clinical study management experience in registries, observational research, RWD/E, or clinical trials as a clinical study lead/project manager.
Deep knowledge of the range of tools used in the clinical study management space and associated technology solutions.
Identify and mitigate risks and apply strong problem-solving skills to ensure timely resolution of all project-related issues.
BA/BS/BScN degree in health or biologic science, or equivalent practical experience.
Master's degree in health or biologic science, or equivalent practical experience.
Program Manager, Study Operations
By Verily At Dallas, TX, United States
Experience in study project management and prior management of contracted resources/CROs.
8+ years of clinical study management experience in registries, observational research, RWD/E, or clinical trials as a clinical study lead/project manager.
Deep knowledge of the range of tools used in the clinical study management space and associated technology solutions.
Identify and mitigate risks and apply strong problem-solving skills to ensure timely resolution of all project-related issues.
BA/BS/BScN degree in health or biologic science, or equivalent practical experience.
Master's degree in health or biologic science, or equivalent practical experience.
Global Ciinical Study Senior Manager
By BeiGene At United States
Mentors more junior team members and might take on line management responsibilities as required
Collaborates with key stakeholders across the organization and provides regular updates on study progress to senior management as required
Leads planning and management of the assigned clinical study(ies) from feasibility through closeout activities
Manages study budgets, including baseline budget evaluation, change control, study closure budget, budget endorsement by senior management
Generates, manages, maintains, and communicates high quality study timelines and tracks progress towards these
Works with the sourcing team to select and manage study vendors, approving invoice payment throughout the study
Preclinical Faculty Jobs
By Touro College of Dental Medicine At New York City Metropolitan Area, United States

Preclinical faculty Mondays and Wednesdays 8-5. D 1 dental student simulation lab, dental anatomy and operative dentistry. Join a great collegial, friendly, dynamic group of faculty staff and ...

Senior Study Manager Jobs
By Clinovo At United States
Required Knowledge, Skills, and Abilities
• Excellent communication and time management skills
Title Manager, Global IST Operations (Interim)
Fully remote – anywhere is US.
******** Title Manager, Global IST Operations (Interim) ************
• Minimum of 3 years of relevant industry experience
Study Manager Jobs
By Altasciences At Kansas, United States
Other tasks as assigned by Study and Departmental Management.
Coordinate operations to meet protocol requirements and pre-defined study timelines. Pro-actively define any needs required to accomplish timelines.
Approve staffing designs and review staffing schedules to ensure sufficient staffing requirements are met based on protocol needs.
Assure the study Investigational Product (IP) is received and dispensed in lieu with study timeline requirements.
3-5 years of experience coordinating clinical trials in a phase one CRO.
Skills: Excellent written and verbal communication, leadership and organizational skills. Customer service focused, able to work in a fast-paced environment.
Preclinical Operations Specialist Jobs
By Vertex Pharmaceuticals At , $45 - $50 an hour
Provides management aspects of outsourced and internal projects including contracting and vendor management
Thinkcell or other project timeline management software
Advanced skills in Microsoft Word and Smartsheet
Meticulous organizational skills and strong attention to detail
Ability to multitask effectively to manage efforts on multiple projects
Possesses computer skills to support and maintain department software programs
Associate Study Start-Up Manager
By BeiGene At , Remote $92,900 - $127,900 a year
Skilled in document management/negotiation and leveraging site relationships to achieve submission targets from start-up through close-out.
Support in management and maintenance of SSU resources (i.e., SSU Toolbox (Americas))
Functional Service Provider model knowledge and/or experience
Project Management - Communicates changes and progress; Completes projects on time and budget.
Demonstrates proficiency of skills required to conduct SSU activities from site identification through activation
Competent in communication and influencing skills to ensure timely follow-up, issue resolution, and report updates
Study Manager - Cardiometabolic
By Merck At United States
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
Building analytical skills to drive operational milestones
Problem solving, prioritization, conflict resolution, and critical thinking skills
Study Project Manager Jobs
By Orion Group At United States
Minimum of 3-5 years of project management experience in the pharmaceutical industry, with a focus on clinical study management
PMP or similar project management certification is preferred
Collaborate with cross-functional teams, including clinical operations, data management, biostatistics, and quality assurance, to ensure seamless study execution
Familiarity with Veeva or other relevant clinical trial management systems
Veeva or similar study management platform
Manage study timelines and ensure that milestones are met on time
Clinical Study Manager - Global
By SRG At United States
• 5 years of study management experience at a sponsor or CRO required
• Working knowledge and experience with Word, PowerPoint, and Excel
• Budget/finance experience on a project level and demonstrates a full understanding of project financials
• Ensure appropriate escalation of issues to Clinical Operations Management
• Phase 1/Clinical Pharmacology CSM experience
• Renal disease experience preferred

Are you looking for an exciting opportunity to manage preclinical studies? We are looking for a Preclinical Study Manager to join our team and help us develop innovative treatments for patients. You will be responsible for the planning, execution, and reporting of preclinical studies, ensuring that all studies are conducted in accordance with applicable regulations and guidelines. If you have experience in preclinical study management and are looking for a challenging and rewarding role, this could be the perfect opportunity for you!

Overview:

A Preclinical Study Manager is responsible for the planning, coordination, and execution of preclinical studies. This includes overseeing the design, implementation, and analysis of preclinical studies, as well as the management of study budgets, timelines, and resources. The Preclinical Study Manager is also responsible for ensuring that all studies are conducted in accordance with applicable regulations and guidelines.

Detailed Job Description:

The Preclinical Study Manager is responsible for the planning, coordination, and execution of preclinical studies. This includes overseeing the design, implementation, and analysis of preclinical studies, as well as the management of study budgets, timelines, and resources. The Preclinical Study Manager is also responsible for ensuring that all studies are conducted in accordance with applicable regulations and guidelines. The Preclinical Study Manager is responsible for the development of study protocols, the selection and management of study sites, the coordination of study activities, and the management of data collection and analysis. The Preclinical Study Manager is also responsible for the preparation of study reports and presentations, as well as the communication of study results to internal and external stakeholders.

What is Preclinical Study Manager Job Skills Required?

• Excellent organizational and project management skills
• Strong knowledge of preclinical study design and implementation
• Ability to develop and manage study budgets
• Ability to develop and manage study timelines
• Ability to develop and manage study protocols
• Ability to select and manage study sites
• Ability to coordinate study activities
• Ability to manage data collection and analysis
• Ability to prepare study reports and presentations
• Ability to communicate study results to internal and external stakeholders
• Knowledge of applicable regulations and guidelines

What is Preclinical Study Manager Job Qualifications?

• Bachelor’s degree in a scientific field
• 5+ years of experience in preclinical study management
• Experience in the pharmaceutical or biotechnology industry
• Knowledge of Good Laboratory Practices (GLP)

What is Preclinical Study Manager Job Knowledge?

• Knowledge of preclinical study design and implementation
• Knowledge of study budgets, timelines, and protocols
• Knowledge of data collection and analysis
• Knowledge of applicable regulations and guidelines
• Knowledge of Good Laboratory Practices (GLP)

What is Preclinical Study Manager Job Experience?

• 5+ years of experience in preclinical study management
• Experience in the pharmaceutical or biotechnology industry

What is Preclinical Study Manager Job Responsibilities?

• Plan, coordinate, and execute preclinical studies
• Oversee the design, implementation, and analysis of preclinical studies
• Manage study budgets, timelines