Study Start-Up Coordinator

Safeguard Global Recruiting; India; On-site; INR 600,000 - 900,000; Full time

Job summary

Safeguard Global Recruiting is seeking a qualified professional to lead and coordinate the study start-up phase within clinical trials. You will collaborate with Project Management and Study Teams to ensure compliant initiation of studies using robust project management practices.

The role requires 2+ years in clinical trials, experience in trial coordination, and knowledge of regulatory submissions. Strong planning, organisation and communication skills are essential for success.

Qualifications

• 2+ years of experience in clinical trials.
• Experience in management or coordination of clinical trials, ideally in an SOM, CRO, NHS trials environment, pharma, or similar setting.
• Knowledge of UK regulatory submissions and trial documentation is advantageous.
• Ability to plan and prioritise workload, handling requests from multiple project managers efficiently.
• Excellent time management, organisation and communication skills.
• Life sciences degree or proven experience in an administration role.

Responsibilities

• Lead and coordinate the study start-up phase in collaboration with the Project Management and Study Teams, ensuring efficient and compliant initiation of standalone studies or programmes through the effective application of project management principles, methodologies, and processes.

Skills

Clinical trials

Project coordination

Time management

Communication

Regulatory knowledge

Education

Life sciences degree

Job description

Lead and coordinate the study start-up phase in collaboration with the Project Management and Study Teams, ensuring efficient and compliant initiation of standalone studies or programmes through the effective application of project management principles, methodologies, and processes

KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:

• At least 2 years’ experience working in clinical trials.
• Demonstrable experience in the management or coordination of clinical trials, ideally gained within a Site Management Organisation, Contract Research Organisation, NHS clinical trials environment, pharmaceutical company, or a comparable setting.
• Knowledge of UK regulatory submissions and Trial documentation would be advantageous.
• Able to plan and prioritise own workload, responding efficiently to requests from multiple project managers.
• Excellent time management, organisation and communication skills
• A life sciences degree/ proven experience in an administration role.