Study Courier Jobs

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

Minimum 6 years or successful execution of over 30 clinical trial studies or collaborative biomedical laboratory study experience (Study Coordinator II)

Preferred experience in managing investigator-initiated, industry-sponsored, or military studies.

Ability to analyze data and summarize findings for incorporation into reports.

The Contractor shall match sponsored studies with appropriate Principal Investigator.

The Contractor shall assure that logs and collected data from patients enrolled in the study remain confidential.

Must have a Bachelors of Science in biomedical science field or nursing

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:

Requirements of protocol from completion to registration of participants.

Completes portions of grant applications &/or documents associated with current local, state, & federal regulatory guidelines, requirements, laws & research protocols.

requirements of protocol from completion to registration of participants.

Reviews & obtains informed consent.

Schedules study visits with participants.

Consults with nurses & physicians to determine pretreatment & eligibility

Required License / Registration / Certification

Assist and monitor student athletes during study hall.

This is a security sensitive position.

Position End Date (if temporary)

Relevant administrative experience including detail oriented, collaborative, positive attitude, ability to prioritize, proactive, and good follow up skills,

Administrative tasks and activities may be requested by a line manager, study team member, or GSO department staff.

Assist with tracking and review of Clinical Trial Insurance requirements, expiry dates, insurance renewal, certificate distribution, and archival

Activities and responsibilities may include:

The SS I is not allocated as a resource to any specific study or program.

BOARD Quarterly MVR GSO Compliance and other metrics

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

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

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:

Oversee data collection, management, and entry into study databases, ensuring accuracy and completeness

Strong knowledge of clinical research processes, regulations, and guidelines.

Excellent organizational, communication, and interpersonal skills.

Collaborate with study teams to develop and implement study protocols, ensuring compliance with regulatory guidelines and ethical considerations

Coordinate participant recruitment and enrollment activities, including screening, selection, and informed consent processes

BA/BS degree in a relevant subject

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

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.

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

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

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

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

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

Education, Qualifications, Skills and Experience

• Good financial management skills.

• Basic change management skills.

Support SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management.

• Excellent understanding of Clinical Study Management and study start-up

Provide regular information to Line Managers at country level on study and planned study milestones/key issues during the start-up period.

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.