Site Activation & Start-Up Lead

IQVIA; Pasig; On-site; PHP 669,600 - 892,800; Full time

Job summary

A leading global provider of clinical research services is seeking a Site Specialist in Pasig, Philippines. The role involves acting as the Single Point of Contact for investigative sites, conducting regulatory start-up and maintenance activities, and ensuring compliance with corporate standards. Ideal candidates will hold a Bachelor's degree in life sciences and possess at least 3 years of clinical research experience. Successful applicants will demonstrate strong negotiation, communication, and organizational skills, contributing to impactful medical treatments.

Qualifications

• 3 years of clinical research or relevant experience.
• In-depth knowledge of clinical systems and corporate standards.
• Ability to apply GCP/ICH and regulatory guidelines.

Responsibilities

• Serve as SPOC for investigative sites in assigned studies.
• Perform regulatory start-up and maintenance activities.
• Negotiate site contracts and budgets with sites.
• Review and ensure compliance with regulatory documents.
• Establish project timelines and ensure efficiency.

Skills

Clinical research experience

Negotiation skills

Effective communication

Organizational skills

Interpersonal skills

Knowledge of GCP/ICH

Ability to work independently

Education

Bachelor’s Degree in life sciences

Job description

A leading global provider of clinical research services is seeking a Site Specialist in Pasig, Philippines. The role involves acting as the Single Point of Contact for investigative sites, conducting regulatory start-up and maintenance activities, and ensuring compliance with corporate standards. Ideal candidates will hold a Bachelor's degree in life sciences and possess at least 3 years of clinical research experience. Successful applicants will demonstrate strong negotiation, communication, and organizational skills, contributing to impactful medical treatments.