Study Start-Up Coordinator(Clinical Trials)

Minerva Research Solutions; Karachi Division; On-site; PKR 1,000,000 - 1,300,000; Full time

Benefits offered by this job

Competitive compensation with rewards

Medical insurance

EOBI retirement benefits

Learning & development opportunities

Paid annual, medical, casual leave

Mental well-being programs

Inclusive, collaborative culture

Recognition & engagement initiatives

Modern digital tools

Job summary

Minerva Research Solutions is seeking a Study Start-Up Coordinator to manage startup timelines and coordinate cross-functional activities for timely SIVs and site activation. You will work closely with Regulatory, QA, Marketing, Finance and Clinical teams to track deliverables and mitigate delays.

Bachelor genetics and related fields or MBBS/BDS/Pharm-D candidates are preferred, with at least 1 year in clinical research or startup coordination.

Qualifications

• Bachelor's degree in Medical Sciences, Life Sciences, Pharmacy or related field.
• MBBS, BDS or Pharm-D candidates preferred.
• Minimum 1 year of experience in clinical research or study startup coordination.
• Familiarity with regulatory requirements and site activation workflows.
• Experience working with cross-functional teams in a fast-paced environment.

Responsibilities

• Track study startup timelines aligned with milestones and activation goals.
• Coordinate cross-functional activities required for study initiation.
• Ensure prerequisites for Site Initiation Visits (SIVs) are completed on time.
• Collaborate with Regulatory, QA, Marketing, Finance and Clinical teams.
• Monitor startup progress and provide regular status updates to stakeholders.
• Identify bottlenecks and elevate risks with recommended mitigations.
• Support readiness for smooth site activation and activation documentation.
• Identify risks and develop contingency strategies for startup activities.

Skills

Project coordination

Communication

Timeline management

Problem solving

Attention to detail

Reporting tools

Education

Bachelor's in Medical Sciences / Life Sciences / Pharmacy

MBBS / BDS / Pharm-D candidates preferred

Job description

Study Start-Up Coordinator

Department: Study Start-Up
Reports To: Compliance Manager
Timings: 6PM - 2AM

About Minerva Research Solutions

Minerva Research Solutions is a leading Clinical Trial Management and Support organization dedicated to advancing global healthcare through innovation, operational excellence, and regulatory compliance. We partner with biotech, pharmaceutical, and healthcare organizations to deliver integrated clinical trial support services across the full study lifecycle.

At Minerva, we are committed to maintaining the highest standards of quality, compliance, and efficiency while enabling breakthrough therapies to reach patients faster.

The Study Start-Up Coordinator is responsible for overseeing study startup timelines and coordinating cross-functional activities to ensure all prerequisites for Site Initiation Visits (SIV) and site activation are completed efficiently and on schedule. This role serves as the central coordination point between departments to monitor dependencies, mitigate delays, and ensure operational readiness for successful study activation.

1. Study Start-Up Planning & Coordination

• Track study startup timelines aligned with project milestones and activation goals.

• Coordinate cross-functional activities required for study initiation.

• Ensure all prerequisites for Site Initiation Visits (SIVs) are completed within timelines.

2. Cross-Functional Alignment

• Coordinate with Regulatory, QA, Marketing, Finance, and Clinical teams to track deliverables and dependencies.

• Identify bottlenecks impacting startup timelines and elevate risks appropriately.

• Facilitate communication between departments to maintain alignment on project objectives and deadlines.

3. Timeline & Milestone Tracking

• Monitor progress against startup timelines using internal tracking tools and dashboards.

• Maintain accurate startup reports and provide regular status updates to stakeholders.

• Proactively address delays and support implementation of corrective actions.

4. SIV Readiness & Site Activation

• Ensure all regulatory, operational, and documentation prerequisites are fulfilled prior to SIV.

• Confirm site activation requirements are completed and appropriately documented.

• Support smooth coordination leading to successful site activation.

5. Risk Management

• Identify potential risks impacting study startup activities and timelines.

• Collaborate with stakeholders to develop mitigation and contingency strategies.

• Monitor ongoing startup risks and ensure timely resolution of issues.

Qualifications & Experience

• Bachelor's degree in Medical Sciences, Life Sciences, Pharmacy, or a related field.

• MBBS, BDS, or Pharm-D candidates will be preferred.

• Minimum 1 year of experience in clinical research or study startup coordination.

• Familiarity with regulatory requirements, clinical trial startup processes, and site activation workflows.

• Experience working with cross-functional teams in a fast-paced environment is preferred.

Key Skills & Competencies

• Strong project coordination and organizational skills

• Excellent communication and stakeholder management abilities

• Ability to manage multiple timelines and priorities effectively

• Strong problem-solving and proactive risk management capabilities

• Attention to detail with a quality-focused mindset

• Proficiency in reporting and startup tracking tools

Key Performance Indicators (KPIs)

• On-time completion of study startup milestones

• Adherence to SIV and site activation timelines

• Number of delays/escalations successfully mitigated

• Effectiveness of cross-functional coordination and communication

• Accuracy and timeliness of startup reporting and tracking

What You'll Gain at Minerva Research Solutions

• Competitive compensation with performance-based rewards

• Comprehensive medical insurance

• EOBI retirement benefits

• Structured Learning & Development pathways, including certifications and career mobility

• Paid annual, medical, and casual leave

• Mental well-being and employee support programs

• Inclusive, collaborative, and growth-driven work culture

• Internal recognition & employee engagement initiatives

• Modern digital tools and a technology-forward workplace

• Transportation allowance for staff

• Family-supportive policies, including parental leave

• Opportunities to contribute to community and social impact programs