Search the 20 jobs at Alimentiv

The Training & Compliance Specialist drives a culture of compliance within Clinical Research, evaluates project quality metrics, leads training initiatives, and supports audits and inspections. Responsibilities may include laboratory assay quality control for the histopathology laboratory.

The Grant Writer will be responsible for identifying and pursuing funding opportunities for research conducted within the Medical R&D group. They will also be involved in writing grant proposals, fostering relationships with funding agencies, and managing grant administration tasks.

Support Project Management, Regulatory, and Legal teams in site start-up activities. Develop relationships with study sites, track start-up progress, and provide project management support. Qualifications include 1-3 years of related experience or a College Advance Diploma/Degree in Health or Life Sciences.

Responsible for leading statistical programming activities for clinical development projects, including development and execution of statistical analysis and reporting deliverables. Provide technical expertise, mentorship, and personnel management. Generate analysis datasets, tables, figures, and listings, review and approve study documents, and support ad-hoc requests.

Provide administrative support to the Medical Imaging department by managing documents, scheduling appointments, and providing clerical services. Assist in project support and corporate administrative tasks to ensure efficient operation of the department.

Seeking an experienced Digital Marketing Manager to support the marketing strategies of a leading clinical research organization. Responsibilities include overseeing digital strategies, website management, marketing automation, campaign management, and social media management. Qualifications include a bachelor's degree in marketing and 5+ years of experience in digital marketing and CRM platform.

Alimentiv is seeking an experienced Full Stack Software Developer to enhance existing products and create innovative solutions for global customers, with a focus on improving human health. The role requires expertise in Node.js, Javascript, Python, HTML, CSS, SQL, cloud-based development, and standard methodologies. Nice-to-have skills include experience with medical imaging, Apache, NGINX, Perl, Scala, AI, and machine learning. The ideal candidate thrives in an innovative environment, completes tasks efficiently, and champions new ideas while adhering to documentation and testing requirements.

Support and coordinate training, compliance, and quality initiatives within Clinical Research. Assist in policy development, training coordination, audits, and communication to ensure compliance and quality standards are met. Responsibilities also include supporting laboratory assay quality control. Requires college diploma/certificate and 1-3 years of related experience, preferably in life sciences/clinical research.

Lead statistical programming activities for clinical research projects, oversee dataset creation, provide technical expertise, mentor junior programmers, and collaborate with sponsors on technical requirements.

Lead statistical programming activities for clinical research projects, oversee study dataset creation, provide technical expertise, mentor junior programmers, and collaborate with sponsors on technical requirements.

Lead statistical programming activities for clinical development projects, generate analysis datasets and reports, provide technical expertise, mentor team members, oversee personnel management, and contribute to process improvement initiatives.

Responsible for providing senior support in planning, organizing, and evaluating the day-to-day delivery of global quality assurance services for Alimentiv Holdings companies. Implements quality assurance plans, oversees QA processes, and ensures compliance with regulatory standards. Provides guidance on product/service enhancements and organizational change. Qualifications include a degree in related field with 4-6 years of experience, knowledge of regulatory standards, analytical skills, and proficiency in Quality Management Systems.

Support all activities related to financial planning & analysis for all company product lines, including revenue and profitability forecasting, cost management, and data analysis. Coordinate with project operational groups to improve financial communications and project financial metrics. Assist in budget forecasts, reconcile project expenditures, develop change orders, and analyze revenue management.

Provide administrative, clerical, and implementation support to project teams and stakeholders. Coordinate meetings, facilitate billing and payment activities, and act as the first point of contact for project queries. Ensure activities align with quality standards and regulatory guidelines.

Seeking an experienced Digital Marketing Manager to support marketing strategies, oversee digital strategies, manage websites, implement SEO strategies, lead marketing automation efforts, and manage social media campaigns.

Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main contact during site start-up. Prepare, distribute, and follow-up on start-up documents with sites. Plan and track site start-up activities and data. Provide reports on study start-up activities.

Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main contact during site start-up. Prepare, distribute, and follow-up on start-up documents with sites. Track site start-up activities and data. Provide reports on study start-up activities.

Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Plan and track site start-up activities and data using designated systems and tools. Provide reports on intelligence and metrics related to study start-up activities.

Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main contact during site start-up. Prepare and track start-up documents, provide reports on study start-up activities, maintain site intelligence tracker, and support project management with study-related activities.

Lead statistical programming activities for clinical development projects, generate analysis datasets and reports, provide technical expertise, mentor team members, oversee personnel management, and participate in process improvement initiatives.