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Study Director Jobs

Study Model Clerk Jobs
By Gainwell Technologies LLC At , Roseville, 95747 $37,500 - $53,500 a year
Manage and track dental models.
Two (2) years prior experience in a dental billing and claims processing environment.
Good communication (oral and written) skills.
Provides dental models to appropriate Dental Professionals for review when the TAR arrives.
Must be a resident of the state of California.
Your role in our mission
Director, Study Start-Up Jobs
By Care Access At United States
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.
Federal Work Study: Grant Researcher
By Teachers College Columbia University At , New York $18 an hour
Assist with website maintenance, communications, and database management
Knowledge and/or experience with sourcing for funding opportunities
Knowledge and/or experience with qualitative research tools
Strong organizational and communication skills
Experience with designing templates on platforms such as CANVA
The general breakdown of responsibilities will be as such:
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.
Study Hall Monitor Jobs
By University of North Texas At , Denton, 76203, Tx $18 an hour
Required License / Registration / Certification
Assist and monitor student athletes during study hall.
This is a security sensitive position.
Position End Date (if temporary)
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
Study Manager - Oncology
By Kelly At Philadelphia, PA, United States
May be responsible for tracking study timelines and will be proficient in project management tools
Pharmaceutical and/or clinical drug development experience beneficial but not required
Demonstrated oral and written communication skills
Excel and PP experience required
BS/BA/MS/PhD with 2+ yrs clinical research experience
Minimum FTE Years of Experience
Onsite Research Study Jobs
By TELUS International AI Data Solutions At Lancaster, CA, United States
Have the legal right to work in the United States.
Be willing to be present in a recorded session.
Are you interested in technology? Do you enjoy contributing to product research?
onsite session in Downtown Los Angeles, California.
$190 for a successful session
Sounds interesting? To participate, please register here:
Local Study Manager Jobs
By Sanofi At Bridgewater, NJ, United States
Certification level of Project Management (PMP/PMI)
Accounts for the set-up, completion, and adaptations of project management tools at country level (CTMS, Control room…)
Be the main link to the local monitoring team in the management of studies
Align on joint KOL/investigator management
Proficiency in complex trial management
Manage and maintain Country Study Budget during course of study
Associate Director Clinical Study Management
By BeiGene At United States
Management experience of CROs, Vendors and Consultants preferred
Ensures the competencies and skills required for the Clinical team is consistent with the company defined requirements
Mentor junior team members to support development by delegating responsibilities, overseeing and supporting development plans
8+ years progressive experience in clinical operations preferably within the biotech, pharmaceutical, and/or CRO environment
Possess understanding of treatment landscape, standard of care, upcoming approvals, and good knowledge of KOLs and investigators
Experience developing trial plans including site monitoring, pharmacy and lab manuals, risk mitigation strategies, trial budgets and site selection/feasibility as required
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.
Director Of Study Start Up
By Tekton Research At Texas, United States
Regularly meet with study team members to collaborate on study date requirements/clarifications, review progress of regulatory submissions, and contract/budget negotiations
Manage and train Source Data Specialists to ensure source is created according to study protocols
Review and approve all source documents created according to protocol and site SOP requirements
5 years clinical research experience
Highly organized and ability to manage multiple studies simultaneously
Previous experience in a study start-up role
Study Coordinator Ii Jobs
By DLH Corporation At Durham, NC, United States
Assist with data collection, electronic data entry and audit checks.
Ability to multi-task and manage time effectively
Ability to pivot to meet changing requirements as needed
Experience drafting regulatory submissions for IRB
Experience with protocol development and consent writing
Experience working at a clinical research site and/or conducting federal clinical research
Study Coordinator Jobs
By DLH Corporation At Bethesda, MD, United States
Experience with adverse event reporting per clinical standards and FDA requirements strongly preferred
Work with Data Managers and Data Team members for forms preparation, and completion of adjudication procedures
Experience working in an academic or NIH research environment preferred
Knowledge of medical terminology preferred
Bachelor's degree req'd with 2 years experience in public health, clinical research or related field.
Implement study activities in accordance with NIH and FDA regulations
Contract Medical Monitor, Usa, Nash Study
By Upsilon Global At United States
NASH experience is preferable, however other associated liver indications also acceptable
To respond to queries related to the protocol and/or enrolment criteria
Act as general medical advisor for any study related issues
Analyse and review data trends
Provide training to study teams
Collaborate and liaise with clinical programme director and wider clinical team
Senior Study Manager Jobs
By Clinovo At United States
Required Knowledge, Skills, and Abilities
• Excellent communication and time management skills
Title Manager, Global IST Operations (Interim)
Fully remote – anywhere is US.
******** Title Manager, Global IST Operations (Interim) ************
• Minimum of 3 years of relevant industry experience
Study Director/Staff Scientist, Ecotoxicology
By Eurofins Lancaster Laboratories At Easton, MD, United States
GLP study director or project management experience required.
Strong computer, scientific, and organizational skills
Bachelor’s degree in relevant field (e.g. biology, zoology, environmental science, marine or fisheries science) with 15 years of experience
A PhD in a relevant field may be substituted for Bachelor’s or Master’s degree and experience.
Study Director responsibilities include, but are not limited to, the following
Completes work for research and development under GLP guidelines for studies, documentation, etc.
Study Coordinator Jobs
By McKesson At Nashville, TN, United States
You will present in weekly protocol meeting to investigators, research staff, and management
You will maintain case report forms tracking management database
You will reports patient visit and data entry information in financial tracking system.
Knowledge of FDA guidelines and GCP is required.
Interpersonal skills, detailed-oriented and meticulous.
Computer skills with ability using clinical trial databases, electronic data capture, MS Access or Excel
Associate Director - Study Abroad
By University of Central Florida At Greater Orlando, United States
Strong written and oral communication skills are key to this position.
Experience with Terra Dotta, Workday, and PeopleSoft is desirable.
Benefit packages, including Medical, Dental, Vision, Life Insurance, Flexible Spending, and Employee Assistance Program
And more…For more benefits information, to go to the UCF Employee Benefits page click here.
Are Benefits Important to You?
Supervises personnel, as assigned. Supervises grant-funded Peace Corps Strategic Recruiter.
Study Manager Jobs
By Altasciences At Kansas, United States
Other tasks as assigned by Study and Departmental Management.
Coordinate operations to meet protocol requirements and pre-defined study timelines. Pro-actively define any needs required to accomplish timelines.
Approve staffing designs and review staffing schedules to ensure sufficient staffing requirements are met based on protocol needs.
Assure the study Investigational Product (IP) is received and dispensed in lieu with study timeline requirements.
3-5 years of experience coordinating clinical trials in a phase one CRO.
Skills: Excellent written and verbal communication, leadership and organizational skills. Customer service focused, able to work in a fast-paced environment.

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?