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Study Director Jobs in Iowa

Director, Study Start-Up Jobs
By Care Access At , Remote
Oversee people management activities including interviewing and selection, terminations, professional development, performance appraisals, job description preparation, and employee counseling.
May support management with site start-up and financial management tasks of projects, as well as strategy development for process improvement.
Proficient with Google Suite and Microsoft Office Suite, and Strong computer skills with demonstrated abilities using clinical trials database.
Oversee Study Start Up Managers and Coordinators, provide guidance and direction, and measure team and individual performance using KPIs.
Expert knowledge of general clinical research processes and Good Clinical Practice.
Ability to build relationships effectively in a geographically dispersed, largely remote environment.
Global Study Management Associate
By BeiGene At , Remote $61,500 - $86,500 a year
Establishes good collaboration with Global Clinical Study Manager, Regional Clinical Trial Management Associates and other key stakeholders globally and regionally
Builds solid knowledge of global clinical trials operations under guidance of the Global Clinical Study Manager
Prepares metrics and updates to key deliverables for management as per information available in relevant systems
Supports management of global study budget incl PO set-up
Project Management - Communicates changes and progress; Completes projects on time and within budget.
Supports the alignment of study goals with clinical operations goals and objectives under direction of the Global Clinical Study Manager
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
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
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

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?