Cto Clinical Trials Project Lead Jobs

4 plus years of experience in clinical trial management

Knowledge of the clinical trial process. Knowledge of ICH guidelines and GCP including basic understanding of regulatory requirements

Oversight and management of day-to-day trial operations including CRO management

Oversight and management of certain sub-studies that may be undertaken from time to time

Management of trials and oversight of day-to-day trial operations (70%)

Management of Study Team Members (15%)

Communicates clinical studies performance data to other members of the management and scientific team.

Ability to lead cross-functional teams and to provide management oversight of CROs.

Experience in developing study budgets, forecasting and financial oversight of a project.

Oversee third party vendors to operationalize the study specifications.

Conducts lessons learned exercises to provide continuous process improvement and sharing of best practices.

Participate in and/or lead departmental initiatives.

Must possess good computer skills and organizational skills. Experience with an electronic document control and management system would be a plus.

Ensure timely and accurate entries and updates into a computer management system required for clinical conduct.

3 or more years of pharmaceutical related experience in medical writing, preferably in a CRO.

Thorough knowledge of International Conference on Harmonization (ICH), Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines.

Strong knowledge of medical terminology, clinical trials, and clinical research.

Strong knowledge of processes with a desire to promote improvement. Ability to motivate and energize others with a positive, can-do attitude.

Effective time management and organizational skills.

Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

Equivalent combination of education, training and experience.

Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.

Knowledge of applicable protocol requirements as provided in company training.

3 years administrative support experience.

🌟 Seeking Talented CTO! Join Our Exciting Journey! 🌟

We want you to bring your expertise to the table and drive our success! 🌐💰

Ready to embrace the challenge? Join us in revolutionizing the rental payments industry!

#CTO #Leadership #Innovation #JoinOurTeam #TechOpportunity

Handle administrative tasks such as billing/invoicing, travel arrangements, event planning, vendor management, presentation development, and spreadsheet management.

Act as a 'Citizen Developer' on tools such as Slack, by leveraging their capabilities to enhance team communication and collaboration.

Drive internal communication within the Technology team, taking detailed meeting notes and disseminating key information to the team.

Maintain and update the Technology team's Confluence page, ensuring all team resources and documents are up-to-date and easily accessible.

Assist with the department's budget, tracking all expenditures and managing requests for funds.

Automate routine tasks wherever possible to improve team efficiency.

Minimum 5 years of combined experience in Medical Affairs/Clinical Operations/Clinical Development

Knowledge of the country’s healthcare system and market access environment

Plan and manage complex projects

Knowledge of clinical trial conduct

Previous experience in rare diseases is of advantage

Ensuring appropriate and compliant level of Patient Advocacy Organization (PAO) group involvement with Patient Advocacy team

Direct the design, development, and maintenance of IRLY's platform, guaranteeing stability, scalability, and a seamless user experience

Assemble, manage, and mentor a top-performing engineering team devoted to delivering best-in-class technology solutions

Develop and manage the engineering budget, efficiently allocating resources to maximize ROI

Minimum of 5 years of experience in software engineering, including mobile and web application development

Comprehensive knowledge of software development methodologies, tools, and technologies

Exceptional problem-solving skills and ability to think strategically and analytically

5+ years of experience in an applied research role

Ph.D. or equivalent experience in training LLMs

Excellent communication and collaborative skills

Establish and continually refine our internal best practices for LLM training

Collaborate with engineers on building state-of-the-art LLM models

Lead research efforts on LLM training, deliver scientific breakthroughs and share these findings at top conferences and through other publication channels

Assist Clinical Research Coordinators in responding to data management queries, monitor findings and follow-up.

Accurately complete research tracking log & LMC Manager ad database

Identify appropriate study candidacy based on knowledge of each sites recruiting and upcoming clinical trials

Work on enrollment and retention initiatives with Manager, Operations and Director of Research

Assist the Director of Research, Manager, Operations and/or Investigators with any other research tasks as required

Perform accurate, complete and timely data entry of electronic or paper case report forms (CRF’s).

Proven experience as a fullstack web developer, software engineer, CTO or similar role

Knowledge of technological trends to build strategy

This is a pre seed position and will be offering equity within a specific timeline

Remote, work from anywhere in the world on your own time.

Develop technical aspects of the company’s strategy and coordinate the building of the B2B marketplace and commodity exchange platform

Discover and implement new technologies that yield competitive advantage

Systematic thinker with strong project management and organizational skills

Experience with modifying, implementing, validating, and maintaining a web-based Clinical Trials Management System, including trouble shooting operational problems

Experience with, or certification in Lean or Six Sigma considered an asset

Recognized certification in clinical research (ACRP or SOCRA) preferred

Minimum five (5) years clinical research experience in a health care setting

Minimum three (3) years cancer related experience

Intermediate computer experience: MS Word, MS Excel, MS PowerPoint, Outlook. Data management experience is desirable.

Minimum of four years clinical trial experience including site monitoring and project coordination responsibilities.

In-depth knowledge of clinical trial and drug development processes; ICH-GCP, FDA and TPD regulatory requirements.

Assists in the development and maintenance of project-specific databases to provide project status reports, historical data and fulfill regulatory requirements.

Demonstrated ability to manage multiple projects and cross-functional teams.

Well-developed interpersonal communication skills, both oral and written.