Senior Program Manager, Study Operations
By Verily At South San Francisco, CA, United States
8-10 years of knowledge and experience working in at least two of the following: project management, clinical research, and software development.
Develop and maintain project artifacts (timeline, project management plan, etc.) that support team communication, efficiency, and regulatory compliance.
Bachelor's degree or equivalent practical experience.
Proven problem-solving and analytical skills, and ability to handle ambiguity.
Strong interpersonal skills with sensitivity to changing personalities and priorities.
Partner with internal product and engineering teams as a passionate advocate for client needs as part of the strategic roadmap.
Home Study And Post Release Services Regional Supervisor (Remote)
By ENDEAVORS At , San Antonio, 78249

Federal Contract Requirements: Provide proof of COVID-19 Vaccination. Must be a U.S. Citizen or a Lawful Permanent Resident. JOB PURPOSE: The Home Study and Post Release Services (HSPRS) ...

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.
Associate Director Study Quality Operations
By Green Key Resources At Greater Boston, United States
Drive continuous improvement and knowledge management by sharing case studies/lessons learned from QA activities to minimize recurrence of similar issues
Significant experience with GxP investigations, risk assessments and CAPA management
Experience with multinational products and regulations as well as with mandated risk management plans
Where applicable provide appropriate quality metrics for established Quality Management Reviews (Global Quality, R&D etc.).
Participate in quality management reviews, risk reviews, and other study/TA/Asset level quality reviews to drive Clinical development and Operations Quality deliverables
Established knowledge of GxP/GCP regulations and guidelines (EMA, FDA, PMDA etc.)
Home Study Writer Jobs
By CK Family Services At , Uvalde, 78801, Tx $275 - $400 a week

Thank you for your interest in partnering with CK Family Services to complete professional assessments of families and children. Specifically, this position is a subcontractor for CK Family Services ...

Study Coordinator Jobs
By UCLA Health At Santa Monica, CA, United States
- 1+ years of experience within clinical research
- Bachelors Degree in related field
- Ability to handle a high volume of trials at a given time
- Oncology clinical research background
Study & Site Operation (Sso) Study Start-Up Country Head, Us - Remote
By Novartis At , East Hanover, 07936, Nj $212,000 - $318,000 a year
Educational minimum requirements: College or university degree with significant life science experience
Manage and supervise productivity targets per defined objectives, and serve as an escalation point for Study Start-Up functions
Strong interpersonal, negotiation and conflict resolution skills
Excellent understanding of all aspects of clinical drug development with particular emphasis on trial set-up, execution, and monitoring
Strong competence in working in a global/country matrix environment
Communicates effectively in a local/global matrixed environment
Study Director Jobs
By TissueVision, Inc At Newton, MA, United States
Strong project management and multi-tasking skills
Experience working in a CRO under a GLP or GLP-like environment
Strong written and oral communication skills
Excellent organizational and problem-solving skills
Experience with molecular or proteomic imaging
Experience with 3D imaging and modeling

Are you looking for a challenging and rewarding opportunity to lead a team of operations professionals? We are seeking an experienced Operations Study Supervisor to join our team and help us achieve our goals. You will be responsible for overseeing the day-to-day operations of our studies, ensuring that all tasks are completed on time and to the highest standards. You will also be responsible for developing and implementing strategies to improve operational efficiency and effectiveness. If you have a passion for operations and a drive to make a difference, this is the job for you!

Overview Operations Study Supervisor is responsible for overseeing the operations of a study or research project. They are responsible for ensuring that the project is conducted in accordance with the study protocol and that all data is collected and reported accurately. They also ensure that the project is completed on time and within budget. Detailed Job Description Operations Study Supervisors are responsible for managing the day-to-day operations of a study or research project. This includes overseeing the recruitment of participants, conducting interviews, collecting and analyzing data, and reporting results. They also ensure that the project is conducted in accordance with the study protocol and that all data is collected and reported accurately. They also ensure that the project is completed on time and within budget. Job Skills Required
• Strong organizational and project management skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Knowledge of research methods and data analysis techniques
• Knowledge of relevant regulations and ethical guidelines
• Proficiency in Microsoft Office and other relevant software
Job Qualifications
• Bachelor’s degree in a relevant field such as psychology, sociology, or public health
• At least two years of experience in a research or study setting
• Knowledge of relevant regulations and ethical guidelines
• Ability to work independently and as part of a team
Job Knowledge
• Knowledge of research methods and data analysis techniques
• Knowledge of relevant regulations and ethical guidelines
• Knowledge of relevant software and databases
Job Experience
• At least two years of experience in a research or study setting
• Experience in project management and data analysis
• Experience in recruiting and interviewing participants
Job Responsibilities
• Oversee the day-to-day operations of a study or research project
• Ensure that the project is conducted in accordance with the study protocol
• Collect and analyze data and report results
• Ensure that the project is completed on time and within budget
• Recruit and interview participants
• Monitor project progress and make adjustments as needed