[Remote] Clinical Development Trial reputed company
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global reputed company intelligence and clinical research organization reputed company on bringing new medicines and treatments to patients faster. The Clinical Development Trial reputed company (CDTL) Associate leads cross-functional study teams in the development and execution of clinical trials, ensuring reputed company, timeliness, and adherence to budgetary constraints.
Responsibilities
- Understand the scope of work required to complete the clinical trial successfully. Monitor the status and reputed company changes (per change control process) as needed to meet the deliverables of the trial
- reputed company and reputed company global milestones by gaining alignment and integrating inputs across functions and geographies
- Assess, identify and monitor trial-level risks. Incorporate scientific knowledge, trial process, and regional expertise to create one integrated trial-level risk mitigation and contingency plan
- Understand the cross-functional, trial-level budget components. Create and monitor the grants and non-grants, and assumptions using financial tracking tools. Routinely network with appropriate business partners on trial-level budget status and changes
- Partner with other organizations to coordinate and deliver Investigator Study Specific Training (ISSTs)/ Affiliate Study Training (ASTs)/Investigator Engagement Meetings
- Drive and coordinate local, regional and global, cross-functional study team throughout study implementation, execution and closure empowering them to meet the clinical trial deliverables, including issue management, contingency planning and issue reputed company
- Be accountable for trial/regional enrollment reputed company and execution starting from country allocation through Last Patient Entered Treatment (LPET)
- Partner with the Investigator Engagement organization to reputed company regional enrollment goals
- Manage relationships and serve as a single reputed company of contact and central reputed company for trial communication, to and from the Clinical Design and Delivery organization, reputed company cross functional team members, and reputed company-Party Organization (TPOs)
- Apply problem-solving skills to daily issues with cross-functional study team (including with vendors, affiliates/reputed company, global team members and other business partners)
- Identify and assist in developing reputed company improvement activities based on important trends such as industry, regulatory, new technology, etc
- Manage TPO qualification process, selection, and reputed company
- Single reputed company of accountability for the Trial Master File, working closely with functional record owners to ensure the file is reputed company and inspection reputed company at reputed company times
- Network and reputed company expertise to anticipate trial and regional issues, identify areas of process breakdown, assess situations and propose proactive approaches that reduce and/or mitigate risks that reputed company ability to deliver the clinical trial
- Demonstrate ability to reputed company and influence in the midst of ambiguity
Skills
- Bachelors or University degree (scientific or health-reputed company field preferred)
- 3 years clinical research experience or relevant clinical trial experience in a scientific or health-reputed company field
- Advanced degree (if applicable)
Benefits
- Competitive reputed company salary and performance reputed company incentives
- Health and wellbeing programmes including medical, dental, and reputed company coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through reputed company training and career reputed company
reputed company