Clinical Study Start-Up Coordinator

Dm Clinical Research Group; Karachi Division; On-site; PKR 900,000 - 1,300,000; Full time

Job summary

Dm Clinical Research Group is seeking a Study Start-Up Specialist to support operational study startup activities across the clinical research network from award to site activation. You will coordinate timelines, track milestones, maintain activation logs, and ensure documentation meets sponsor and internal requirements.

You will work with Regulatory, Clinical Operations, Clinical Data, sponsors, CROs, investigators, and site teams to keep startup deliverables on track and escalate issues as

Qualifications

• 1–3+ years of clinical research, startup coordination, regulatory support, or clinical operations experience
• Experience coordinating multiple tasks and priorities in a fast-paced operational setting
• Experience working within a clinical research site, CRO, sponsor, or research network environment
• ACRP or SOCRA certification preferred but not required

Responsibilities

• Support startup activities across assigned studies and network sites from study award through activation
• Track startup timelines, deliverables, milestones, and outstanding action items
• Maintain startup trackers and activation logs
• Coordinate follow-up on pending startup tasks, approvals, and documentation
• Escalate delays or barriers to SSU leadership appropriately
• Support onboarding and training of new SSU team members as assigned

Skills

Organizational skills

Communication skills

Team collaboration

Attention to detail

Task management

Education

Associate's or Bachelor's degree in Life Sciences, Healthcare Administration, Business Administration, or related field

Tools

Microsoft Office Suite

Google Workspace

Startup tracking systems

Job description

Dm Clinical Research Group is seeking a Study Start-Up Specialist to support operational study startup activities across the clinical research network from award to site activation. You will coordinate timelines, track milestones, maintain activation logs, and ensure documentation meets sponsor and internal requirements.

You will work with Regulatory, Clinical Operations, Clinical Data, sponsors, CROs, investigators, and site teams to keep startup deliverables on track and escalate issues as