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Administrator, Office Management
Summary:
We are seeking a highly independent and motivated Office All-Rounder to join our clinical research company as an integral part of our office operations. This position requires a full-time presence in the office and offers the opportunity to contribute to various aspects of office management, adminisEmployment Type: Full-time
Experience Level: Associate
Clinical Regional Project Lead
Summary:
In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across Asia Pacific region. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders. The scope of responEmployment Type: Full-time
Experience Level: Mid-Senior Level
Clinical Regional Project Lead
Summary:
In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across Asia Pacific region. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders. The scope of responEmployment Type: Full-time
Experience Level: Mid-Senior Level
Clinical Regional Project Lead
Summary:
In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across Asia Pacific region. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders. The scope of responEmployment Type: Full-time
Experience Level: Mid-Senior Level
Site Management Associate (SMA)
Summary:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products, while taking a step further in your professional careeEmployment Type: Full-time
Experience Level: Entry Level
Site Technology Specialist
Summary:
Provides clinical sites with technical support and expertise related to technology. Assists in the design and implementation of study related forms, guidelines and manuals related to technologies. Coordinates data collection related to technologies, including but not limited to nuclear medicine, radEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Research Pharmaceuticals
Director, Business Development
Summary:
We are looking for a Director of Business Development who will expand our existing client base in the United States. Actively prospects and leverages potential new business opportunities within specified Customer/Accounts. Cultivates strong, long-term relationships with key decision-makers with AccoEmployment Type: Full-time
Experience Level: Director
Site Management Associate I
Summary:
Hybrid role in Durham, NC Site Management Ensures exchange of information and documentation with sites and vendors Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies Ensures regulatory and ethics committee submissions and notifications EnsuEmployment Type: Full-time
Experience Level: Associate
Site Management Associate I
Summary:
Hybrid role in King of Prussia, PA Site Management Ensures exchange of information and documentation with sites and vendors Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies Ensures regulatory and ethics committee submissions and notificatEmployment Type: Full-time
Experience Level: Associate
Study Startup Specialist II
Summary:
Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time. This is an office-based position from our Bangalore office . You will: Collaborate with the project team fEmployment Type: Full-time
Experience Level: Associate
Lead Clinical Research Associate
Summary:
Coordinates investigator/ site feasibility and identification process, as well as study startup. Monitors project timelines and patient enrollment, implements respective corrective and preventive measures. Reviews monitoring visit reports for all visit types and ensures reporting compliance of the MEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Management Pharmaceuticals
Lead Clinical Research Associate
Summary:
Coordinates investigator/ site feasibility and identification process, as well as study startup. Monitors project timelines and patient enrollment, implements respective corrective and preventive measures. Reviews monitoring visit reports for all visit types and ensures reporting compliance of the MEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Management Pharmaceuticals
DevOps Engineer
Summary:
In this role, you will be responsible for building, maintaining, and optimizing infrastructure, CI/CD pipelines, and deployment processes across multiple environments. Full-time permanent employment in Kazakhstan Key Responsibilities Troubleshoot system issues using logs, diagnostics, and monitoringEmployment Type: Full-time
Experience Level: Associate
DevOps Engineer
Summary:
In this role, you will be responsible for building, maintaining, and optimizing infrastructure, CI/CD pipelines, and deployment processes across multiple environments. Full-time permanent employment in Estonia Key Responsibilities: Troubleshoot system issues using logs, diagnostics, and monitoring tEmployment Type: Full-time
Experience Level: Associate
DevOps Engineer
Summary:
In this role, you will be responsible for building, maintaining, and optimizing infrastructure, CI/CD pipelines, and deployment processes across multiple environments. Key Responsibilities Troubleshoot system issues using logs, diagnostics, and monitoring tools Develop and maintain automation scriptEmployment Type: Full-time
Experience Level: Associate
Site Management Associate
Summary:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. This role is based in Athens, Greece Communication and Site Management Exchanges data, documents and other project relevant informatEmployment Type: Full-time
Experience Level: Associate
Data Manager for Clinical Trials
Summary:
Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for. Please submit your CV in English Responsibilities will inclEmployment Type: Full-time
Experience Level: Associate
Tags: Analyst Pharmaceuticals
Data Manager for Clinical Trials
Summary:
Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for. Please submit your CV in English Responsibilities will inclEmployment Type: Full-time
Experience Level: Associate
Tags: Analyst Pharmaceuticals
Data Manager for Clinical Trials
Summary:
Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for. Please submit your CV in English Responsibilities will inclEmployment Type: Full-time
Experience Level: Associate
Tags: Analyst Pharmaceuticals
Site Management Associate I
Summary:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Only CVs in English will be accepted. You will be responsible for: Being the main point of contact between site personnel and CRA inEmployment Type: Full-time
Experience Level: Entry Level
Clinical Trials Import/Export Operations Specialist
Summary:
Please submit your CV in English. Be the point of contact with customs authorities, courier companies, and carriers for different issues and negotiation Stay abreast of changes in import or export laws/regulations Classify goods according to the tariff coding system Manage, track, maintain and revieEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Lead Clinical Research Associate
Summary:
As a Lead Clinical Research Associate, you will hold a leadership role within the study team, overseeing and guiding the clinical team while driving trial activities at a country or regional level. You will ensure high-quality execution, compliance, and timely delivery. You will act as a key point oEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals