Our mission is to ensure the generation of accurate and precise findings.
Contact Us Ta-134/A, Gulshan Badda Link 61 383 766 284 noreply@envato.com
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Our mission is to ensure the generation of accurate and precise findings.
Contact Us Ta-134/A, Gulshan Badda Link 61 383 766 284 noreply@envato.com
At S4 Research we see our personnel as "Ambassadors" of our company and our sponsors and so we treat them accordingly with the respect and investment such a crucial role demands.
Our expert team is at the heart of our organisation and our most valuable asset and we are extremely committed to identifying, developing and retaining individuals as part of our truly dynamic and innovative team.
As it is in our direct interest to work with highly motivated team members, we place great impetus on comprehensive training, development and career advancement of our personnel to ensure they reach their full potential. We strive to attain the highest quality in everything we undertake and therefore we are seeking personnel that express a conscientious attitude and take pride in their work. With good communication, organisational and interpersonal skills we are looking for experienced, independent and pro-active individuals.
S4 Research is actively hiring across India! We are looking for talented professionals with strong communication and site management skills to join our fast-growing team.
Requirements:
Minimum 3 years of experience in Monitoring, Quality Assurance, or Site Management
Proven ability to manage clinical sites effectively
Excellent communication and collaboration skills
Fill out the form below and upload your CV to take the next step in your career with S4 Research.
S4 is seeking a skilled IT Support Specialist to oversee and manage day-to-day IT operations across the organization. The ideal candidate will have hands-on experience with key IT systems and a proactive approach to problem-solving and documentation.
Key Responsibilities:
Manage and support daily IT operations
Administer Office 365, including user accounts and access management
Maintain and troubleshoot cloud servers and internal platforms
Develop, update, and maintain IT SOPs and user manuals
Support and manage SharePoint and company website
Provide technical support to internal teams and ensure system reliability
Required Qualifications:
Minimum 3 years of experience in IT support or systems administration
Strong hands-on experience with Office 365, cloud infrastructure, and user access management
Familiarity with IT SOPs, process documentation, and internal IT compliance
Excellent troubleshooting and communication skills
Experience with SharePoint and web site management
Submit your details and upload your CV to become part of S4’s growing team.
S4 is looking for experienced Study Coordinators across India to support clinical trial activities at the site level. This role is crucial to ensuring protocol compliance, quality data collection, and coordination between investigators and study teams.
Key Responsibilities:
Coordinate day-to-day clinical trial activities at the study site
Ensure compliance with study protocols, GCP, and regulatory requirements
Support patient recruitment, screening, and informed consent processes
Maintain accurate and timely study documentation (source documents, ISFs, E-CRF, logs, etc.)
Required Qualifications:
Minimum 1 year of experience as a Study Coordinator or in clinical trial site management
Strong understanding of GCP, ICH guidelines, and regulatory requirements
Excellent organizational and communication skills
Bachelor's degree in life sciences, pharmacy, nursing, or related field
Fill out the form and upload your CV to apply.
S4 Research is seeking a highly organized and results-driven Project Manager to lead clinical trial projects. This role includes coordinating with investigator sites and Sponsor/CRO teams, driving patient recruitment, overseeing overall site management, and managing teams of site coordinators and site operations specialists. The Project Manager will ensure sites are audit-ready at all times, proactively manage risks, escalate issues promptly, and maintain the highest quality of deliverables throughout the project lifecycle.
Required Qualifications:
Minimum 5 years of project management experience in clinical research
Proven experience managing and leading teams of site coordinators and operations staff
Strong understanding of clinical trial processes, GCP, and regulatory environment
Excellent communication, leadership, and problem-solving skills
PMP certification or equivalent is a plus
Bachelor’s degree in life sciences, healthcare, or related discipline
Send us your profile. Fill the form below: