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 ...
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 · 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 ...
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 Project Director at Allucent, you are responsible for overseeing and managing all aspects of the clinical study trials for Neuroscience or Immunology and Infectious Diseases . Experience in Cell ...
As a Project Director at Allucent, you are responsible for overseeing and managing all aspects of the clinical study trials for Neuroscience or Immunology and Infectious Diseases . Experience in Cell ...
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 ...
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 ...
Director, CMC
Cary, NC · Remote
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 ...
Director, CMC
Cary, NC · Remote
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 ...
The role In this role, you'll be responsible for setting the department strategy and overall utilization and profitability of Allucent Medical Affairs and Pharmacovigilance. This position controls ...
The role In this role, you'll be responsible for setting the department strategy and overall utilization and profitability of Allucent Medical Affairs and Pharmacovigilance. This position controls ...
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 ...
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 ...
Senior Technology System Integeration Engineer
Minneapolis, MN · On-site
$109K - $149K/yr
Experience with at least one or more scheduling technologies (OPC, P6, Microsoft Project, Allucent, Planera) • ETL & Scripting: Utilize API connectivity, error management and other methods to ...
Senior Technology System Integeration Engineer
Minneapolis, MN · On-site
$109K - $149K/yr
Experience with at least one or more scheduling technologies (OPC, P6, Microsoft Project, Allucent, Planera) • ETL & Scripting: Utilize API connectivity, error management and other methods to ...
Senior Technology System Integeration Engineer
Minneapolis, MN · On-site
$100K - $135K/yr
Experience with at least one or more scheduling technologies (OPC, P6, Microsoft Project, Allucent, Planera) ETL & Scripting: Utilize API connectivity, error management and other methods to automate ...
Senior Technology System Integeration Engineer
Minneapolis, MN · On-site
$100K - $135K/yr
Experience with at least one or more scheduling technologies (OPC, P6, Microsoft Project, Allucent, Planera) ETL & Scripting: Utilize API connectivity, error management and other methods to automate ...
Allucent information
What is Allucent and what does the company do?
Allucent is a global contract research organization (CRO) that specializes in providing clinical development services to small and mid-sized biotechnology and pharmaceutical companies. The company supports drug development throughout the clinical trial process, including study design, regulatory support, data management, and medical writing. Allucent focuses on helping clients bring new therapies to market efficiently by leveraging scientific expertise and tailored solutions for complex clinical trials.
What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Allucent, and why are they important?
To thrive as a Clinical Research Associate, you need a solid background in life sciences or a related field, along with knowledge of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and often a certification such as ACRP or SOCRA is highly valuable. Strong attention to detail, organizational skills, and effective communication are crucial soft skills for managing trials and collaborating with multidisciplinary teams. These competencies ensure high-quality trial execution, compliance, and reliable results in the dynamic environment of clinical research.
What types of clinical research projects do Allucent team members typically work on, and how do they collaborate within project teams?
At Allucent, team members typically work on early-phase to late-phase clinical trials, often focusing on small to mid-sized biotech and pharmaceutical clients. Projects can range from first-in-human studies to post-marketing surveillance, with a strong emphasis on innovative therapies. Collaboration is central to Allucent's approach—project teams usually include clinical project managers, clinical research associates, data managers, and regulatory experts who work closely together using digital platforms and regular meetings to ensure project milestones are met efficiently and compliantly.
What is the difference between Allucent vs Clinical Research Coordinator?
| Aspect | Allucent | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, often in health or science fields; certifications like CCRP or RAC beneficial | Bachelor's degree in health, science, or related field; certifications like CCRP or CCRC often preferred |
| Work Environment | Pharmaceutical and biotech research settings, often in labs or offices | Clinical trial sites, hospitals, or research centers |
| Employer & Industry Usage | Biotech, pharmaceutical companies, and research organizations | Hospitals, clinics, research institutions, and contract research organizations |
Allucent primarily focuses on clinical research services within biotech and pharmaceutical industries, often involving data management and regulatory support. Clinical Research Coordinators (CRCs) are directly involved in managing clinical trial activities at research sites. While both roles require similar credentials and work in the clinical research industry, Allucent roles tend to be more specialized in research support services, whereas CRCs are hands-on in trial execution at clinical sites.
More about Allucent jobs
What cities are hiring for Allucent jobs?
Cities with the most Allucent job openings:
What states have the most Allucent jobs?
States with the most job openings for Allucent jobs include:
What job categories do people searching Allucent jobs look for?
The top searched job categories for Allucent jobs are:
- Director Cmc Regulatory Affairs
- Regulatory Affairs Diagnostics
- Vp Regulatory Affairs Remote
- Vice President Of Regulatory Affairs
- Regulatory Affairs Director Biotech
- Vice President Cmc Regulatory Affairs
- Director Regulatory Affairs
- Associate Director Regulatory Affairs Cmc
- Regulatory Affairs Contractor
- Aurobindo Pharma Regulatory Affairs
Job description
At Allucentâ„¢, 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 Project Director (PD) to join our A-team (office-based*/remote). 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 (GCO) department. This position controls and monitors the quality and full-service delivery of clinical trial Allucent customers.
About this role:
As a proactive project director, you will:
Requirements
To be successful, you will posess:
Benefits
Benefits of working at Allucent include:
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
We are looking for a Project Director (PD) to join our A-team (office-based*/remote). 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 (GCO) department. This position controls and monitors the quality and full-service delivery of clinical trial Allucent customers.
About this role:
As a proactive project director, you will:
- Oversee the project and be responsible for the overall quality and management of the deliver clinical trial projects and programs. This includes overseeing the budget, reviewing and approving content and costing of proposals, problem solving with project teams, and balancing multiple competing priotities.
- Serve as the key contact for assigned clients on delivery of scope, customer satisfaction on services and capabilities and the assessment of client needs.
- Lead the project team. You will demonstrate knowledge of and insight into general business principles and practices, demonstrate a growth mindset, and support the recruitment and interviewing of new employees.
Requirements
To be successful, you will posess:
- Minimum Bachelor's degree in life science, healthcare and/or business degree; Master's degree or greater preferred
- Minimum 8 years of relevant work experience, specifically experience in drug development and/or clinical research ; CRA experience preferred.
- Minimum 8 years of project management experience, specifically as a clinical project manager ; managing global clinical trials required
- Extensive clinical project management experience, with at least 5 years of clinical project management experience
- Expert knowledge of ICH-GCP(R3), data and patient privacy practices, and applicable (local) regulatory requirements
- Strong financial acumen, administrative excellence and analytical skills
- In some cases, an equivalency-consisting of a combination of appropriate education, training, and/or directly related experience-will be considered appropriate for an individual to meet the requirements of this role
- Therapeutic expertise in Oncology required
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