Clinical Trial Lead
Cary, NC · Remote
As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...
Quick apply
21 Allucent Jobs Hiring Near You
Clinical Trial Lead
Cary, NC · Remote
As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...
As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial ...
As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial ...
Clinical Trial Lead
Cary, NC · On-site
As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...
Clinical Trial Lead
Cary, NC · On-site
As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...
Chez Allucent, nous nous engageons a aider les petites et moyennes entreprises biopharmaceutiques a naviguer efficacement dans l'univers complexe des essais cliniques afin d'offrir des traitements ...
Chez Allucent, nous nous engageons a aider les petites et moyennes entreprises biopharmaceutiques a naviguer efficacement dans l'univers complexe des essais cliniques afin d'offrir des traitements ...
$11.50 - $15.50/hr
As Allucent, you will coordinate and support local site start-up activities of Allucent Study Start-up & Site Intelligence. This may include essential record collection, Independent Ethics Committee ...
$11.50 - $15.50/hr
As Allucent, you will coordinate and support local site start-up activities of Allucent Study Start-up & Site Intelligence. This may include essential record collection, Independent Ethics Committee ...
Chez Allucent , nous nous engageons a aider les petites et moyennes entreprises biopharmaceutiques a naviguer efficacement dans le monde complexe des essais cliniques afin d'apporter des traitements ...
Chez Allucent , nous nous engageons a aider les petites et moyennes entreprises biopharmaceutiques a naviguer efficacement dans le monde complexe des essais cliniques afin d'apporter des traitements ...
Clinical Trial Lead
Cary, NC · On-site +1
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across ...
Clinical Trial Lead
Cary, NC · On-site +1
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across ...
As a PD at Allucent, you are responsible for coordinates and oversees operational project teams, customer satisfaction and continuous improvement of processes within the Global Clinical Operations ...
As a PD at Allucent, you are responsible for coordinates and oversees operational project teams, customer satisfaction and continuous improvement of processes within the Global Clinical Operations ...
Clinical Trial Lead
Cary, NC · On-site +1
As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...
Clinical Trial Lead
Cary, NC · On-site +1
As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...
NY · On-site
When you work at Allucent, that means applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments. If ...
As a Medical Director/Sr. Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent ...
As a Medical Director/Sr. Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent ...
Directeur medical adjoint-oncologie/ Associate Medical Director-Oncology (CAN)
Montreal, QC · On-site
Chez Allucent, nous nous engageons a aider les petites et moyennes entreprises biopharmaceutiques a naviguer efficacement dans l'univers complexe des essais cliniques afin d'offrir des traitements ...
Directeur medical adjoint-oncologie/ Associate Medical Director-Oncology (CAN)
Montreal, QC · On-site
Chez Allucent, nous nous engageons a aider les petites et moyennes entreprises biopharmaceutiques a naviguer efficacement dans l'univers complexe des essais cliniques afin d'offrir des traitements ...
Start-Up Associate/Sr. Start-Up Associate - Contractor (USA)
$16 - $21.50/hr
As Allucent, you will coordinate and support local site start-up activities of Allucent Study Start-up & Site Intelligence. This may include essential record collection, Independent Ethics Committee ...
Start-Up Associate/Sr. Start-Up Associate - Contractor (USA)
$16 - $21.50/hr
As Allucent, you will coordinate and support local site start-up activities of Allucent Study Start-up & Site Intelligence. This may include essential record collection, Independent Ethics Committee ...
As an Associate Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent, serving as ...
As an Associate Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent, serving as ...
When you work at Allucent, that means rolling up your sleeves and applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life ...
When you work at Allucent, that means rolling up your sleeves and applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life ...
QC · On-site
Chez Allucent, nous nous engageons a aider les petites et moyennes entreprises biopharmaceutiques a naviguer efficacement dans l'univers complexe des essais cliniques afin d'offrir des traitements ...
En tant que directeur médical adjoint chez Allucent, vous serez chargé de veiller, de manière autonome, à l'intégrité et à la qualité des aspects médicaux, cliniques et de sécurité des ...
Quick apply
En tant que directeur médical adjoint chez Allucent, vous serez chargé de veiller, de manière autonome, à l'intégrité et à la qualité des aspects médicaux, cliniques et de sécurité des ...
As an Medical Director/ Sr. Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent ...
Quick apply
As an Medical Director/ Sr. Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent ...
En tant que CTL chez Allucent, vous assurez le leadership, la gestion et la supervision des chargés d'étude clinique (CRA) et des autres équipes cliniques dans le cadre de leurs activités ...
Quick apply
En tant que CTL chez Allucent, vous assurez le leadership, la gestion et la supervision des chargés d'étude clinique (CRA) et des autres équipes cliniques dans le cadre de leurs activités ...
As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial ...
As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial ...
Allucent Jobs Information
Job description
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the 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. The CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and with quality.
ResponsibilitiesAs an expert in Clinical Trial Leadership, you are:
- Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Manager and other functional leads to ensure clinical monitoring deliverables (timeline, budget, quality, productivity) are met.
- Liaising closely with the Project Manager (PM) and other department leaders if /when necessary, on all trial-related issues and service delivery.
- Supporting the management team with training, process improvements, co-monitoring visits, mentoring of staff and / or any other special assignments within Global Clinical Operations.
Requirements
To be successful you will possess:
- A degree in life sciences or nursing qualification preferred, but not required.
- A minimum of 5 years of clinical research experience with at least 2-years’ CTL or other relevant experience.
- In-depth knowledge of ICH GCP, clinical trials and the critical elements for success in clinical trials
- Strong therapeutic background in oncology
- Possesses experience and knowledge in the CRO industry that will support Allucent’s management of clinical trials
- Strong written and verbal communication skills including professional command of English language to communicate with internal and external stakeholders on a daily basis.
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 (within reason)
- Opportunity for remote/hybrid* working depending on location
- 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 2 days in office per week for employees within reasonable distance from one of our global offices.
“The Allucent Talent Acquisition 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