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
Regulatory Coordinator Iii/Clinical Researcher
By Cedars-Sinai At West Hollywood, CA, United States
Completes forms and generates all reports necessary to comply with regulatory requirements and institutional policies.
Establishes and maintains research files and documentation pertaining to regulatory requirements for clinical research/clinical trials.
May provide training and education to other personnel.
Participates in required training and education programs.
Five (5) years minimum of directly related experience; 2 years of regulatory experience and 3 years of clinical research experience.
Ability to identify areas of project interest and connect with appropriate support group: CCTO SPIN, IRB, Tech Transfer
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.
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.
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.
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 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.
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

Are you looking for an exciting opportunity to make a real difference in the world of clinical research? We are seeking a Clinical Trial Researcher to join our team and help us develop innovative treatments for patients. As a Clinical Trial Researcher, you will be responsible for designing and executing clinical trials, analyzing data, and reporting results. You will have the opportunity to work with leading medical professionals and be part of a team that is making a real impact in the medical field. If you are passionate about clinical research and want to make a difference, this is the job for you!

Overview:

Clinical Trial Researchers are responsible for the design, implementation, and analysis of clinical trials. They work with medical professionals to ensure that the trials are conducted in accordance with the highest standards of safety and efficacy. They also collaborate with other researchers to ensure that the data collected is accurate and reliable.

Detailed Job Description:

Clinical Trial Researchers are responsible for designing, implementing, and analyzing clinical trials. They work with medical professionals to ensure that the trials are conducted in accordance with the highest standards of safety and efficacy. They also collaborate with other researchers to ensure that the data collected is accurate and reliable. They must be able to interpret and analyze the data collected from the trials and present their findings in a clear and concise manner. They must also be able to communicate effectively with medical professionals, other researchers, and sponsors of the trials.

What is Clinical Trial Researcher Job Skills Required?

• Knowledge of clinical trial design and implementation
• Knowledge of medical terminology and clinical trial protocols
• Ability to interpret and analyze data
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to work under pressure and meet deadlines
• Proficiency in Microsoft Office Suite

What is Clinical Trial Researcher Job Qualifications?

• Bachelor’s degree in a related field such as biology, chemistry, or public health
• Master’s degree in a related field such as clinical research, epidemiology, or biostatistics
• Certification in clinical research (CCRP)
• Experience in clinical research or related field

What is Clinical Trial Researcher Job Knowledge?

• Knowledge of clinical trial design and implementation
• Knowledge of medical terminology and clinical trial protocols
• Knowledge of data analysis and interpretation
• Knowledge of regulatory requirements for clinical trials

What is Clinical Trial Researcher Job Experience?

• Previous experience in clinical research or related field
• Experience in data analysis and interpretation
• Experience in clinical trial design and implementation

What is Clinical Trial Researcher Job Responsibilities?

• Design and implement clinical trials in accordance with the highest standards of safety and efficacy
• Collaborate with medical professionals and other researchers to ensure accuracy and reliability of data collected
• Interpret and analyze data collected from the trials
• Present findings in a clear and concise manner
• Communicate effectively with medical professionals, other researchers, and sponsors of the trials
• Ensure compliance with regulatory requirements for clinical trials