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Clinical Trial Management Jobs in San Francisco, California

Clinical Trial Research Nurse I
By Kaiser Permanente At , San Francisco $148,200 - $191,730 a year
With supervision, assist in the accurate and appropriate study test article management.
Support the effective financial management of the clinical trial.
Other duties as assigned by appropriate management.
Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.
With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.
No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.
Clinical Trial Manager Jobs
By 89bio At San Francisco, CA, United States
Experience in CRO selection and management including drafting request for proposals (RFPs), bidding process, etc.
Conduct Site Qualification Visits (SQVs) to assess investigator's staff, capabilities, and facilities
In-depth knowledge of FDA regulatory requirements and medical practice/techniques and terminology
Select and manage vendors (including CROs, central lab, etc.)
Manage investigational product supply at study and site levels
Work with Clinical Research Organizations (CROs) to ensure coordination of Sponsor and CRO responsibilities, obligations are being met
Clinical Trial Manager Jobs
By SciPro At South San Francisco, CA, United States
**This opportunity may have future direct management responsibilities.
Manage vendor operational meetings to ensure project goals and timelines are met.
Early phase and start up experience required.
Demonstrated experience in selecting, managing, overseeing, and successfully developing effective relationships with multiple vendors and CROs.
Prior experience working in a start-up environment is a highly desired.
Responsible for study start-up, including working with cross functional teams on startup, and with the CRO on site selection/activation
Senior Clinical Trial Assistant
By Theery At Redwood City, CA, United States
Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:
Maintain and manage requests for access to and deactivation of study systems users.
Competency of the drug development process with knowledge of ICH-GCP is a plus
Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills
Distribute safety alerts and relevant documents, if required
Maintain and update study team and vendor contact information
Clinical Trial Budget Negotiation Analyst - Remote
By UC San Diego Health At , San Diego $75,000 - $95,000 a year
Seven (7) years of related experience, education/training, OR a Bachelor’s degree in related area plus three (3) years of related experience/training.
Thorough knowledge of finance policies, practices, and systems.
Thorough knowledge and understanding of internal control practices and their impact on protecting University resources.
Demonstrated experience analyzing and drafting complex clinical trial budgets and negotiating mutually satisfying terms and conditions.
#122969 Clinical Trial Budget Negotiation Analyst - Remote
Candidates hired into this position may have the ability to work remotely.
Trial Attorney Jobs
By US Securities and Exchange Commission At , Los Angeles, 90071 $163,744 - $272,100 a year
If you are relying on your education to meet qualification requirements:
All qualification requirements must be met by the closing date of this announcement.
DRUG TESTING: This position may be subjected to drug testing requirements.
You will be evaluated for this job based on how well you meet the qualifications above.
CITIZENSHIP: This position is open to US Citizens.
You must possess a J.D. or LL.B Degree.
Project Manager – Clinical Trial Management Systems
By OSI Engineering At Oakland, CA, United States
Previous clinical trials experience in a similar role providing project management, solutions management, and IT solutions to a clinical trials program.
IT project management experience related to implementing and optimizing components in clinical trial digital ecosystems.
5+ years of experience in system design/ architecture project manager/ related position.
Provide support and manage areas of System Design/ Architecture.
Experience working with Tableau or similar analytic reporting software.
Experience working on any kind of benchmarking and/ or milestone reporting software to show metrics and progress.
Clinical Trial Management Associate
By Ionis Pharmaceuticals, Inc. At Carlsbad, CA, United States
Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and distributes management reports from internal tracking systems at requested intervals
Assists with the tracking and management of study specific budgets
Assists with facilitating resolution of data queries and requests from Clinical Data Management
Critically evaluates job tasks and the impact on overall trial management objectives
Collaborates with the Clinical Trial Manager and/or the Clinical Project Lead on the development of certain study-specific plans and/or processes
Prepares investigational site reference materials (i.e., screening/enrollment logs, Delegation of Site Responsibilities form, Site Monitoring Log, etc.)
Clinical Trial Associate Jobs
By Actalent At San Diego Metropolitan Area, United States
Inform the Clinical Operations Manager/Project Team on any outstanding document(s).
Support the Clinical Operations Manager(s) coordinating project meetings, including scheduling and drafting, distribution, and filing of meeting agendas and minutes.
Experience in managing eTMF platforms in an outsourced environment is required, with a minimum of 2 years of experience strongly preferred.
Understanding and working knowledge of regulations and standards applied in clinical areas, medical devices, and/or pharmaceutical products is required.
Strong skills with Microsoft Excel and SharePoint are required.
Communicate effectively with clinical study administration vendors (Functional Service providers etc.).
Clinical Trial Manager Jobs
By Amgen At Thousand Oaks, CA, United States
Previous managerial experience directly managing people and/or experience in leading teams, projects, programs or directing the allocation of resources
High school diploma/GED and 12 years of Manufacturing & Operations experience OR
Associate’s degree and 10 years of Manufacturing & Operations experience OR
Bachelor’s degree and 5 years of Manufacturing & Operations experience OR
Master’s degree and 3 years of Manufacturing & Operations experience OR
Solid knowledge of downstream, as well as a general knowledge of the associated analytical and buffer preparation techniques
Global Clinical Trial Manager (Us-Remote)
By Amgen At Santa Clara, CA, United States
Analyze your business effectiveness of sales activities and territory analysis, as well as develop territory plans with your District Manager
Three or more years of sales and/or marketing experience within pharmaceutical, biotech, healthcare, or medical device industries.
Flexible work models, including remote work arrangements, where possible
Craft an effective marketing strategy to aid in driving sales
Leverage your passion for Oncology and disease state awareness, Industry, regulatory and competitive changes to deliver agreed results
A Bachelor's degree in Life Sciences or Business Administration.
Clinical Trial Rater Jobs
By M3 USA At Los Alamitos, CA, United States
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Clinical Trial Manager/Sr. Clinical Trial Manager
By Akero Therapeutics At San Francisco Bay Area, United States
Relevant clinical trial experience in the pharmaceutical or health care industry or equivalent
Experience as the regional lead for Europe, United States, and/or India.
Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable
This position is for remote work, but may require domestic or international travel as required (valid travel documents must be obtainable).
At least 4+ years of relevant experience and a BS or BA in a relevant scientific discipline OR
Clinical Trial Management Associate
By Akero Therapeutics At San Francisco Bay Area, United States
Accountable for study level tracking as assigned by the Clinical Project Manager; e.g. monitor visit tracking and sample tracking.
At least 2+ years of relevant experience and a BS or BA in a relevant scientific discipline OR
At least 2+ years of experience and an RN (2 or 3 year certificate)
Relevant clinical trial experience in the pharmaceutical or health care industry or equivalent
Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable
Clinical Trial Assistant-1 Jobs
By Cue Health At San Diego, CA, United States
Effective organizational and time management skills; ability to manage multiple assignments and changing priorities
Demonstrate commitment to the implementation and effectiveness of Cue’s Quality Management System
Knowledge of applicable clinical research regulatory requirements (e.g., GCP and ICH GCP)
Create, manage, and audit clinical trial master files and investigator site binders
A minimum of 1 year of experience in clinical research or related field
Previous experience in creating, managing, and auditing clinical trial master files and investigator site binders
Clinical Trial Rater Jobs
By M3 USA At Los Angeles, CA, United States
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Clinical Trial Assistant Jobs
By Corcept Therapeutics At Menlo Park, CA, United States
Assist project team with study specific documentation including filing to the Clinical Trial Management System and Trial Master File
Preferred Skills, Qualifications and Technical Proficiencies:
Track clinical supply inventory at sites and manage the site drug re-supply process
Set-up and maintain tracking system with oversight of manager
Develop working knowledge of company standard operating procedures (SOPs) and FDA regulations related to clinical studies
Familiarity with applicable regulatory requirements, Good Clinical Practice/ICH and Good Documentation Practices
Clinical Trial Assistant (Cta)
By Cytokinetics At , South San Francisco, 94080, Ca $31.50 - $38.50 an hour
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Assistant (Cta)
By Cytokinetics At South San Francisco, CA, United States
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Assistant Jobs
By Abbott Laboratories At , San Diego, Ca $24 - $49 an hour
To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
To provide general administrative support to the Clinical Affairs Department and assistance to department Manager(s) and Director(s).
Research or health care related academic or work experience preferable.
Good written and verbal communication skills.
To assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals.

Do you want to make a difference in the lives of patients? Join our team as a Clinical Trial Manager and help us bring innovative treatments to the world!

Overview of Clinical Trial Management Clinical Trial Management is a specialized field of healthcare that involves the management of clinical trials. Clinical Trial Managers are responsible for the planning, coordination, and execution of clinical trials. They work with research teams, sponsors, and regulatory agencies to ensure that clinical trials are conducted in accordance with applicable regulations and standards. Clinical Trial Managers are also responsible for the development of protocols, the recruitment of participants, and the collection and analysis of data. Detailed Job Description of Clinical Trial Management Clinical Trial Managers are responsible for the planning, coordination, and execution of clinical trials. They work with research teams, sponsors, and regulatory agencies to ensure that clinical trials are conducted in accordance with applicable regulations and standards. Clinical Trial Managers are responsible for developing protocols, recruiting participants, and collecting and analyzing data. They must also ensure that all safety and ethical standards are met. Clinical Trial Managers must be able to effectively communicate with research teams, sponsors, and regulatory agencies. They must also be able to manage budgets and timelines. Clinical Trial Management Job Skills Required
• Knowledge of clinical trial regulations and standards
• Excellent communication and organizational skills
• Ability to manage budgets and timelines
• Ability to work independently and as part of a team
• Knowledge of data collection and analysis methods
• Knowledge of safety and ethical standards
Clinical Trial Management Job Qualifications
• Bachelor’s degree in a related field
• Experience in clinical research or clinical trial management
• Certification in clinical trial management (preferred)
• Knowledge of applicable regulations and standards
Clinical Trial Management Job Knowledge
• Knowledge of clinical trial regulations and standards
• Knowledge of data collection and analysis methods
• Knowledge of safety and ethical standards
• Knowledge of applicable regulations and standards
Clinical Trial Management Job Experience
• Experience in clinical research or clinical trial management
• Experience in budget and timeline management
• Experience in working with research teams, sponsors, and regulatory agencies
Clinical Trial Management Job Responsibilities
• Develop protocols for clinical trials
• Recruit participants for clinical trials
• Collect and analyze data from clinical trials
• Ensure that safety and ethical standards are met
• Manage budgets and timelines for clinical trials
• Communicate with research teams, sponsors, and regulatory agencies