Clinical Trials Management Associate Jobs in Arkansas

Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role

Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)

Strong organizational and problem-solving skills

Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

Skill sets and proven performance equivalent to the

Maintain and quality audit to assure the most recent revisions of documents are on project portals

Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management

Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role

Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)

Strong organizational and problem-solving skills

Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)

Working with vendors and vendor managers to ensure efficient collection of requirements for clinical supply chain functions.

Develop budget overviews based off vendor management, clinical systems and logistics team inputs.

Relevant degree or equivalent education within business or finance area.

Ideally experience working within pharmaceutical or biotech environment, or alternatively working within a supplier or procurement group.

Experience within budgeting and invoice tracking.

Some knowledge of supply chain processes would be advantageous.

Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management

Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role

Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)

Strong organizational and problem-solving skills

Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)

● Knowledge of clinical operations, project management tools and processes.

● Delegates and manages tasks and responsibilities to other team members assigned to the study

● In collaboration with data management, facilitates ongoing data review in preparation for interim,

judgment along with the ability to recommend business alternatives to senior management

This is a remote position with occasional travel.

● At least 6 years of clinical research experience including at least three (3) years having effectively