Coordinate and conduct multiple clinical research studies according to protocol, including subject recruitment, consenting, and administration of protocol required procedures.
Responsibilities
Coordinate and conduct multiple clinical research studies according to protocol
Recruit and consent study subjects
Administer protocol required procedures such as questionnaires, vital sign measurements, biospecimen collection, follow up contacts
Collect accurate clinical data from subject interviews, medical record review, and study indicated procedures
Enter data into appropriate data management systems
The Senior Issue Lead will be accountable for managing confirmed Major / Critical Quality Event cases through investigation, root cause analysis, CAPA management, and inspection coordination, ensuring compliance and quality standards.
Compensation
The annual base salary for this position ranges from $162,900.00 to $271,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program.
Responsibilities
Manage confirmed Major / Critical Quality Event cases through investigation and root cause analysis
Ensure investigations meet timelines and compliance requirements
Direct QE team in proposing and documenting Corrective and Preventative Actions
Present complex cases to senior leaders as part of the Quality Review Team
Coordinate GCP related audits and inspections
Requirements
BA/BS
MBA/MS
Nice to have: Master’s degree
Nice to have: scientific background in Life Sciences
Assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Compensation
Competitive base salary and performance related incentives
Responsibilities
Coordinate study documents, trackers, meetings and operational requests
Maintain accurate study information in relevant systems and repositories
Support site and study team communications and follow up
Track actions, milestones and outstanding documentation
Apply study procedures and escalate issues promptly
Requirements
Bachelor's degree in a scientific or healthcare-related field
Nice to have: ICH Good Clinical Practice (GCP) training
Nice to have: Clinical trial management systems (CTMS)
As a Senior CRA, you’ll play a critical role in ensuring clinical studies are conducted with the highest standards of quality, patient safety, and regulatory compliance. Your expertise will help drive the successful execution of studies from site qualification through closeout, supporting the delivery of reliable data that advances clinical research.
Compensation
United States of America - $97,000.00 - $193,000.00
Responsibilities
Manage clinical research activities at investigative sites participating in Worldwide clinical studies
Identify and assess potential research sites to support successful study execution
Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes
Conduct all types of monitoring visits: Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs), Interim Monitoring Visits (IMVs) and Closeout Visits (COVs)
Train site personnel on protocol requirements, data collection processes, and safety reporting expectations
As a Senior CRA, you’ll play a critical role in ensuring clinical studies are conducted with the highest standards of quality, patient safety, and regulatory compliance. Your expertise will help drive the successful execution of studies from site qualification through closeout, supporting the delivery of reliable data that advances clinical research.
Compensation
United States of America - $97,000.00 - $193,000.00
Responsibilities
Manage clinical research activities at investigative sites participating in Worldwide clinical studies
Identify and assess potential research sites to support successful study execution
Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes
Conduct all types of monitoring visits: Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs), Interim Monitoring Visits (IMVs) and Closeout Visits (COVs)
Train site personnel on protocol requirements, data collection processes, and safety reporting expectations
Clinical Research Associate II responsible for designing and analysing clinical trials, monitoring sites, ensuring protocol compliance, and maintaining data integrity.
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolve queries to maintain high-quality clinical data
Prepare and review study documentation, including protocols and clinical study reports
Requirements
Bachelor's degree in a scientific or healthcare-related field
Senior Clinical Research Associate responsible for designing, monitoring, and analyzing clinical trials, ensuring protocol compliance, data integrity, and patient safety.
Responsibilities
Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolve queries to maintain high‑quality clinical data
Prepare and review study documentation, including protocols and clinical study reports
Requirements
Bachelor's degree in a scientific or healthcare‑related field
