Independently manage and monitor investigator sites through initiation to database lock, ensure GCP/regulatory compliance, lead site activation, resolve complex site issues, implement CAPAs, mentor CRAs, support inspections and audit remediations, oversee safety reporting and investigational product handling, and collaborate cross-functionally to support enrollment and data quality.
Why This Role Matters
Are you ready to take your monitoring expertise to the next level and mentor the next generation of clinical research professionals? As a Senior Clinical Research Associate I (SCRA I), you will oversee site management, monitoring, and close-out operations for assigned clinical trials with a higher level of accountability and operational judgment.
In addition to driving patient safety and trial quality, you will serve as a Subject Matter Expert (SME), contribute to regional process improvements, and partner directly with Site Care Partners (SCPs) on early-phase activation activities. Your deep therapeutic insight and leadership will directly safeguard trial integrity, strengthen crucial investigator relationships, and enhance Pfizer's scientific credibility with global external stakeholders.
The Impact You Will Make
In this senior-level role, you will take on expanded operational and mentorship responsibilities:
• Advanced Monitoring & Site Management: Independently manage and monitor assigned investigator sites from initiation to database lock. Ensure compliance with Study Monitoring Plans, SOPs, GCP guidelines, and prevailing laws.
• Site Activation & Preparation: Partner with Site Care Partners prior to site activation on crucial feasibility and site selection processes, Pre-Trial Assessments (PTAs), site activation checklists, Informed Consent Document (ICD) finalization, and Site Initiation Visits (SIVs).
• Leadership & Mentorship: Actively mentor and train Clinical Research Associates (CRAs) as assigned, supporting their development and operational capability.
• Subject Matter Expertise: Serve as a Subject Matter Expert (SME) for CRA-related processes and participate in regional or local working groups and process improvement initiatives.
• Issue Resolution & Compliance: Identify, resolve, and manage complex investigator site issues. Establish and implement robust CAPAs, manage Quality Event remediations, support sponsor regulatory interactions/inspections, and drive Audit Observation CAPA developments.
• Collaborative Partnerships: Partner with SCPs, Country SOMs, Clinicians, Recruitment Specialists, and Clinical Data Scientists. Provide enrollment support, address complex protocol inquiries, and conduct remote assessment of e-diary data.
• Quality Oversight: Monitor site-level AEs/SAEs, collaborate with the Drug Safety Unit, handle investigational product oversight (accounting, storage, destruction), support database release, and conduct co-monitoring activities as requested.
What You Bring
• Education: Bachelor's degree in Life Sciences, or a professional degree in nursing, pharmacy, medical background, or equivalent.
• Core Knowledge: Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA, and local country regulations.
• Experience: Minimum of 3 years of relevant experience in clinical research site monitoring (with a preference for 2 years of experience in Oncology).
• Global Exposure: Prior global clinical trial experience is required.
• Language Skills: Fluency in English and the native language(s) of the country you will work in.
• Preferred Experience: Therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases.
Key Skills :
• Advanced knowledge of clinical R&D operational elements (monitoring, data acquisition, cleaning, and reporting).
• Demonstrated ability to support sponsor regulatory inspections/interactions and protocol design/feasibility processes.
• Proven ability to work in a matrix environment, influence stakeholders, and lead through others.
• Advanced analytical capacity to interpret complex data and support risk management.
Work Schedule, Travel & Environment
• Travel Commitment: This role requires significant travel (60% to 80%) within your assigned area. Occasional international and weekend travel may be required.
• Requirements: A valid driver's license and passport are required.
Work Location Assignment: Remote
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.
Digital Transformation Strategy
One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
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.
Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
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
Are you ready to take your monitoring expertise to the next level and mentor the next generation of clinical research professionals? As a Senior Clinical Research Associate I (SCRA I), you will oversee site management, monitoring, and close-out operations for assigned clinical trials with a higher level of accountability and operational judgment.
In addition to driving patient safety and trial quality, you will serve as a Subject Matter Expert (SME), contribute to regional process improvements, and partner directly with Site Care Partners (SCPs) on early-phase activation activities. Your deep therapeutic insight and leadership will directly safeguard trial integrity, strengthen crucial investigator relationships, and enhance Pfizer's scientific credibility with global external stakeholders.
The Impact You Will Make
In this senior-level role, you will take on expanded operational and mentorship responsibilities:
• Advanced Monitoring & Site Management: Independently manage and monitor assigned investigator sites from initiation to database lock. Ensure compliance with Study Monitoring Plans, SOPs, GCP guidelines, and prevailing laws.
• Site Activation & Preparation: Partner with Site Care Partners prior to site activation on crucial feasibility and site selection processes, Pre-Trial Assessments (PTAs), site activation checklists, Informed Consent Document (ICD) finalization, and Site Initiation Visits (SIVs).
• Leadership & Mentorship: Actively mentor and train Clinical Research Associates (CRAs) as assigned, supporting their development and operational capability.
• Subject Matter Expertise: Serve as a Subject Matter Expert (SME) for CRA-related processes and participate in regional or local working groups and process improvement initiatives.
• Issue Resolution & Compliance: Identify, resolve, and manage complex investigator site issues. Establish and implement robust CAPAs, manage Quality Event remediations, support sponsor regulatory interactions/inspections, and drive Audit Observation CAPA developments.
• Collaborative Partnerships: Partner with SCPs, Country SOMs, Clinicians, Recruitment Specialists, and Clinical Data Scientists. Provide enrollment support, address complex protocol inquiries, and conduct remote assessment of e-diary data.
• Quality Oversight: Monitor site-level AEs/SAEs, collaborate with the Drug Safety Unit, handle investigational product oversight (accounting, storage, destruction), support database release, and conduct co-monitoring activities as requested.
What You Bring
• Education: Bachelor's degree in Life Sciences, or a professional degree in nursing, pharmacy, medical background, or equivalent.
• Core Knowledge: Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA, and local country regulations.
• Experience: Minimum of 3 years of relevant experience in clinical research site monitoring (with a preference for 2 years of experience in Oncology).
• Global Exposure: Prior global clinical trial experience is required.
• Language Skills: Fluency in English and the native language(s) of the country you will work in.
• Preferred Experience: Therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases.
Key Skills :
• Advanced knowledge of clinical R&D operational elements (monitoring, data acquisition, cleaning, and reporting).
• Demonstrated ability to support sponsor regulatory inspections/interactions and protocol design/feasibility processes.
• Proven ability to work in a matrix environment, influence stakeholders, and lead through others.
• Advanced analytical capacity to interpret complex data and support risk management.
Work Schedule, Travel & Environment
• Travel Commitment: This role requires significant travel (60% to 80%) within your assigned area. Occasional international and weekend travel may be required.
• Requirements: A valid driver's license and passport are required.
Work Location Assignment: Remote
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.
Digital Transformation Strategy
One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
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.
Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
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
Similar Jobs at Pfizer
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Lead design, delivery and maintenance of GMP/GDP audit strategy for biologics, aseptic, small molecule and medical device areas. Plan and execute complex audits, coach auditors, analyze regulatory intelligence, drive corrective actions, support inspection readiness, and partner with PGS/PharmSci and site stakeholders to ensure compliance and continuous improvement.
Top Skills:
Aseptic ManufacturingDigital HealthEu DirectiveFdaGdpGmpIchIsoMedical Device RegulationsPic/SQuality Management SystemSoftware As A Medical Device (Samd)Tga
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Senior Clinical Research Associate II leads clinical monitoring to ensure GCP compliance, patient safety, and data quality across investigator sites. Duties include site management (on-site/remote), mentoring CRAs, performing SCP tasks for small projects, driving process improvements, preparing for audits/inspections, coordinating with safety/regulatory teams, and managing site performance with frequent travel.
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Lead International Commercial Digital & AI portfolio and commercial-model innovation across Top16 and Cluster markets. Own portfolio governance, investment decisions, business cases, benefits tracking, partnership strategy, FIT accelerator rules, and market-sensing inputs. Drive reuse discipline, model cost visibility, go/no-go gates, and scale proven use cases while influencing senior stakeholders across a global matrix.
Top Skills:
Agentic TechnologyAISpark
What you need to know about the Dublin Tech Scene
From Bono and Oscar Wilde to today's tech leaders, Dublin has always attracted trailblazers, with more than 70,000 people working in the city's expanding digital sector. Continuing its legacy of drawing pioneers, the city is advancing rapidly. Ireland is now ranked as one of the top tech clusters in the region and the number one destination for digital companies, with the highest hiring intention of any region across all sectors.
