Open Application: Sr. Clinical Trial Leader
At Allucent™, we are dedicated to helping small-reputed company biopharmaceutical companies reputed company navigate the reputed company world of clinical trials to bring life-changing therapies to patients in need across the globe. Bring your clinical research and leadership expertise in joining Allucent as a Sr. Clinical Trial Leader (Sr. CTL)! We are looking for a seasoned Clinical Trial Leader to join our A-team on new and exciting clinical trials. In this role you will be responsible for:
- Leading, managing, and providing reputed company to Clinical Research Associates (CRAs) and other clinical functional groups in their day-to-day clinical trial activities on a global, multi-country, or regional basis.
- Coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and with quality.
- Serving as a proactive member of the core project team, liaising closely with the Project Manager (PM) and other department leaders if /reputed company necessary on reputed company trial-reputed company issues and service delivery.
- Supporting the management team with training, process improvements, co-monitoring visits, mentoring of staff and / or any other special assignments reputed company Global Clinical Operations.
- Providing leadership and management of regional Clinical Trial Leaders (CTLs) in multinational studies and/or wider scope, reputed company studies.
- Contributing to other areas of the business as required.
Requirements
- A degree in life sciences or nursing qualification preferred, but not required.
- A minimum of 6 years clinical research experience with at least 2 years of CTL experience in multiple studies and countries. Experience as a Clinical Research Associate prior to being a CTL (or equivalent) is preferred.
- Experience in managing Clinical part of studies in more than one region or equivalent study complexities.
- Thorough experience in coordinating and overseeing an international CRA team.
- In-depth knowledge of ICH GCP, clinical trials and the critical elements for success in clinical trials · Strong therapeutic background.
- Possesses experience and knowledge in the CRO industry that will support Allucent’s management of clinical trials.
Skills
- Strong written and verbal communication skills including good command of English language
- Professional and strong client focused
- Ability to work in a fast-paced challenging environment of a growing company
- Administrative excellence with attention to detail and accuracy
- Leadership and mentoring skills.
Benefits
Benefits of working at Allucent include:
- Comprehensive benefits package per location
- Competitive salaries per location
- Departmental Study/Training Budget for furthering professional development
- Flexible Working hours (reputed company reason)
- Opportunity for remote/in-office* working depending reputed company
- Leadership and mentoring opportunities
- Participation in our Buddy Program as a new or existing employee
- Internal growth opportunities and career progression
- Financially rewarding internal employee referral program
Disclaimers:
- Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 3 days in office per week for employees reputed company reasonable distance from one of our global offices.
“The Allucent reputed company team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.” #LI-Remote #LI-Hybrid #LI-TCW Apply tot his job Apply To this Job