Senior Clinical Research Associate

Role Summary

The Senior Clinical Research Associate is responsible for the site management, site monitoring, and closeout of assigned clinical trial investigator sites to ensure patient safety and quality study execution in accordance with applicable regulations, Good Clinical Practice (GCP), and Pfizer standards.

The role is accountable for managing investigator site relationships, ensuring effective delivery of clinical trials, safeguarding site quality and compliance, supporting enrollment and database release activities, and maintaining strong engagement with investigators and site staff. The Senior Clinical Research Associate works closely with Site Care Partners and study team members throughout study start-up, execution, and closeout.

Key Responsibilities

Manage and monitor assigned investigator sites throughout the clinical trial lifecycle.

Ensure studies are conducted in accordance with protocol requirements, applicable regulations, GCP, and Pfizer standards.

Serve as the primary point of contact for assigned investigator sites during study conduct.

Partner with Site Care Partners and study teams to support site performance and quality delivery.

Support site activation, patient recruitment, enrollment, and study progress.

Conduct on-site, remote, and electronic monitoring visits, including site initiation, routine monitoring, and closeout visits.

Review and follow up on adverse events (AEs) and serious adverse events (SAEs) as required.

Maintain study documentation, monitoring reports, follow-up letters, protocol deviation records, and Trial Master File documentation.

Identify site-level issues and implement corrective and preventive action plans when necessary.

Resolve data queries and support database release activities.

Ensure appropriate oversight of investigational product management at investigator sites.

Participate in investigator meetings as required.

Support audit readiness and quality event remediation activities when applicable.

Additional Responsibilities

Mentor and train Clinical Research Associates, as assigned.

Serve as a subject matter expert for CRA-related processes.

Participate in regional, local, or global process improvement initiatives.

Support Site Care Partner activities related to feasibility assessment, site selection, site activation planning, and study startup activities.

Conduct co-monitoring activities when required.

Qualifications

Bachelor's degree in Life Sciences or an equivalent healthcare-related discipline such as Nursing, Pharmacy, or Medicine.

Extensive knowledge of clinical trial methodologies, ICH/GCP requirements, FDA regulations, and local country regulations.

Minimum 3 years of clinical research site monitoring experience.

Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases.

Global clinical trial experience.

Fluency in English and the local language(s) of the country of employment.

Knowledge, Skills and Competencies

Strong knowledge of clinical research and clinical development processes.

Strong understanding of regulatory requirements and clinical trial operations.

Ability to evaluate, interpret, and communicate complex clinical and operational issues.

Ability to work effectively in a matrix environment.

Strong communication and stakeholder management skills.

Ability to support regulatory inspections and audits.

Understanding of protocol development, feasibility assessment, and risk management activities.

Travel Requirements

Significant travel is required.

Occasional international and weekend travel may be required.

Valid driver's license and passport require

Work Location Assignment: Remote - Field Based

Purpose

Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.

School of Leaders

We, as Pfizer Turkey, make a difference with our visionary and pioneering approaches ranging from our concept of raising leaders through rotations, providing international career opportunities to creating a flexible, enjoyable work environment. There are no limits to what we can accomplish to touch lives here!

Flexibility

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!

Equal Employment Opportunity

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on  Pfizer Careers .

Medical