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Study Director Jobs

Associate Study Director - Fully Remote!!
By The Jackson Laboratory At Bar Harbor, ME, United States
Excellent management/supervisory project management and project oversight skills and proven experience with mentoring direct reports.
Knowledge and experience in using process improvement techniques and approaches such as lean six sigma preferred.
Excellent oral and written communication skills.
Demonstrated ability to develop and lead technical teams.
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.)
Burn Research Study Assistant
By University of Washington At , Seattle, 98195, Wa $3,260 - $3,757 a month
Experience with basic laboratory techniques and sample processing (pipetting, centrifuging, sample shipments).
Our Commitment to Equity, Diversity, and Inclusion
All staff in the Department of Surgery are asked to demonstrate and develop the following core competencies:
Quality Focus: strives to deliver the best possible service and results, and continuously seeks opportunities for improvement.
Planning & Organization: completes work in a timely, efficient, and resourceful manner
Teamwork & Relationship Building: builds and fosters positive working relationships with others to achieve shared objectives.
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
Data Analyst (Work-Study) Jobs
By University of Utah At , Salt Lake City, 84112, Ut $10 - $15 an hour
Physical Requirements and Level of Frequency that may be required
Non Benefited Staff / Student
1 year or more, but less than 2 years
2 years or more, but less than 4 years
4 years or more, but less than 6 years
Appropriate discharge document (such as a DD-214 – Member Copy 4) – Veteran Only – Call 801.581.2169
Literature Study Guide Writer
By SuperSummary At , Remote $200 - $900 a week
Fully remote/flexible work schedule - As a freelancer, you work the hours you want from anywhere on the globe
Experience with literary analysis and/or academic writing
Teaching or tutoring experience is a huge plus!
Prompt weekly payments - Transparent, competitive rates for each assignment
Performance incentives - Exceed our expectations and timelines to earn a bonus on each assignment
Tiered rates - Writers who write reliably and well earn higher rates
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 Guide Writer (Non-Fiction)
By SuperSummary At United States
Fully remote/flexible work schedule - As a freelancer, you work the hours you want from anywhere on the globe
Experience with academic writing and/or teaching
Prompt weekly payments - Transparent, competitive rates for each assignment
Performance incentives - Exceed our expectations and timelines to earn a bonus on each assignment
Tiered rates - Writers who write reliably and well earn higher rates
Consistent and reliable work on the subject matter you love most and know best
Director, Lester E. Fisher Center For The Study And Conservation Of Apes
By Lincoln Park Zoological Society At , Chicago, 60614, Il $90,000 - $100,000 a year
Applied knowledge of principals of research methods, animal behavioral observations, data collection and analysis.
Demonstrated knowledge and expertise in one or more areas of non-human primate biology.
Strong interpersonal, communication and conflict resolutions skills with the ability to create and maintain a productive work culture.
Exceptional written and verbal skills including ability to engage varying audiences in the work of the center
Ph.D. with demonstrated knowledge and expertise in one or more areas of non-human primate biology.
Salary dependent upon experience, range $90K-100K/year
Director, Study Administration Jobs
By Centricity Research At United States
Experience or certification in clinical trial management, project management, and data management activities
2 years of management experience
Provide oversight on completion of administrative tasks across multiple databases and project management systems.
Liaise with Leadership, Clinical Operations, Clinical Data Systems, Business Development, Finance, QMS, Human Resources, and Marketing/Recruitment team leads as necessary.
5 years-experience in clinical research
5 years-experience with Centricity Research
Study On Gender And Water Resource Management
By CTG Global UAE - Committed To Good At , Remote
How can women knowledge & experiences be shared for the upscaling of good practices & interventions?
What are best practices, or previous good examples during which women participated in WRM including resolving water conflicts or water management?
Education Qualifications of National Consultant:
Demonstrated experience in/excellent knowledge and understanding of Yemen country context, national key stakeholders are considered an asset.
Data collection as per the approved inception report & allocation of responsibilities as agreed with the International Consultant.
In-depth experience working in conflict-affected countries.
Research Study Coordinator Jobs
By Boston Medical Center At , Remote
Demonstrated progressive work experience in research management and project planning
Support file management, storage, and tracking across relevant Cores and study teams
Ability to learn and assimilate other related computer applications into study and data management practices
At least 2 years relevant experience required. Experience in clinical research, public health experience, project coordination or training programs preferred.
Exceptional verbal/written English communication skills, including excellent grammatical, editing and proofreading skills
Advanced skills with Microsoft applications (Outlook, Word, PowerPoint) and other web-based applications. Ability to learn and implement new software systems
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
Rn Study Coordinator Jobs
By Mayo Clinic At , Jacksonville, 32224, Fl $28.50 - $42.80 an hour
Rate of Pay Based on Education :
Graduate of an accredited Bachelor's degree Nursing program.
Associates- $28.50 - $42.80 / hour
Bachelors- $32.09 - $48.19 / hour
Affirmative Action and Equal Opportunity Employer
Federal Work Study Literacy Tutor
By Saybrook University At , Remote $17 an hour
Position responsibilities include, but are not limited to:
Assist teachers and administration with general office duties.
Be a current student in good standing at Saybrook University
Be a current volunteer with a school who is interested in partnering with Saybrook University
Be available to volunteer up to 20 hours per week
Eligible for Federal Work Study
Military Analyst (Future Study Program)
By Army Futures Command At Newport News, VA, United States

Duties Summary About the Position: The incumbent will serve as a Military Analyst (Future Study Program) for the US Army, Futures and Concepts Center, Directorate of Concepts, Fort ...

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 an exciting and rewarding opportunity to lead a team of scientists and researchers? We are looking for a Study Director to join our team and help us develop innovative solutions to complex scientific problems. You will be responsible for overseeing the design, implementation, and analysis of experiments and studies, as well as providing guidance and direction to the research team. If you have a passion for science and a desire to make a difference, this could be the perfect job for you!

A Study Director is a professional who is responsible for the design, implementation, and management of clinical trials. They are responsible for ensuring that the trial is conducted in accordance with the protocol, Good Clinical Practice (GCP) guidelines, and applicable regulations. They are also responsible for the safety and well-being of the study participants. To become a Study Director, one must have a degree in a relevant field, such as medicine, nursing, or life sciences, and experience in clinical research. Additionally, they must have strong organizational, communication, and problem-solving skills. Study Director skills include knowledge of clinical trial design, GCP guidelines, and applicable regulations; experience in clinical research; strong organizational, communication, and problem-solving skills; and the ability to manage multiple projects simultaneously. Study Director knowledge includes clinical trial design, GCP guidelines, and applicable regulations; clinical research methods; and data analysis. Study Director responsibilities include designing and managing clinical trials; ensuring compliance with GCP guidelines and applicable regulations; monitoring the safety and well-being of study participants; and analyzing and interpreting data. Study Director experience includes working in a clinical research setting and managing clinical trials. Study Director qualifications include a degree in a relevant field, such as medicine, nursing, or life sciences, and experience in clinical research. Study Director education includes courses in clinical trial design, GCP guidelines, and applicable regulations. Tools that help Study Directors work better include project management software, data analysis software, and electronic data capture systems. Good tips to help Study Directors do more effectively include staying organized, communicating clearly, and staying up-to-date on GCP guidelines and applicable regulations. Common Study Director interview questions include: What experience do you have in clinical research? How do you ensure compliance with GCP guidelines and applicable regulations? What strategies do you use to manage multiple projects simultaneously?