Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for people.
At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.

Site Activation Partner

The Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Pfizer standards. Responsibility within a country and may span over more than 1 country depending on the geographical region and business needs.

 

ROLE RESPONSIBILITIES

 Initiate and coordinate activities and essential documents management during start-up towards the compilation of a high-quality Investigator Initiation Package (IIP) leading to approval for site initiation

 Register investigator sites and Pfizer stakeholders in Pfizer registries and systems as required. Update and regularly maintain the registry with accuracy and have it inspection ready

 Work directly and interact with investigator sites to confirm readiness for site start-up by reviewing study site profile ready in SIP or reviewing/completing critical information Sheet inclusive of but not limited to Investigator Initiation Packages (IIP) essential documents components, Site contracts contacts, clinical supply shipment information, payment information, IRB submission and status

 Take the lead to resolve issues or concerns and timely escalation of Site issues where applicable

 Prepare, validate and submit regulatory documents such as completed IIP, IRB approval forms, FDA 1572/Attestation Form, for internal regulatory approval within required timelines

 Manage and coordinate with other supporting roles to ensure timely site activation and operational activities.

 Support the compilation of the Central Investigator Review Board (IRB) package and submissions to approval of the study (where applicable) and other committees as per country requirements

 Coordinate the timely communication, documentation and responses between Pfizer and Central Ethics committee to bring clinical study to approval (country dependent)

 Support investigators sites with local IRB workflow from preparation, submission through approval

 Assist with preparation, handling and distribution of non-Clinical Trial Supplies and maintenance of tracking information as needed

 Collaborate with the Study Team on the development and readiness of sites eISF when utilized and act as primary point of contact for the sites and manage the Site Operations/CRO monitor access to eISF prior to SIV.

 

Assist with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.

 Support & implement activities in Shared Investigator Platform to align with Pfizer strategy as it relates to the role

 Coordinate translation of documents that are within scope with the preferred translation vendors Clinical Trials Conduct

 Post site activation, initiate and coordinate activities and essential documents management with the investigator’s sites towards the compilation of a high-quality documents and updates through the life cycle of a study such as the documents management for protocol amendments, FDA 1572/Attestation revisions, Ethics Committee annual approvals and other activities required during study conduct

 Ensure maintenance of IRB/Ethics and other committees’ activities as applicable

 Responsible for timely filing of documents to Trial Master File and assisting with periodic quality review of study files for accuracy and completeness

 Accurately update and maintain clinical trial systems that track site compliance and performance within project timelines

 Supports investigator sites, and study teams in preparation for and providing responses to site audits / inspections Internal & External Communication

 Maintain ongoing contact and communication with the study team and respond promptly to study team and investigator site requests

 Attend study Start-up meeting and provide functional updates on a country and site level

 Establish tools for efficient updates to study team as needed regarding site status, issues, delays, approvals

 Disseminate Central or Local Ethics Approval to study team and Investigator Sites where applicable

 Communicate Local sites approvals to study team members and stakeholders Clinical Trial Site Support

 As needed, perform, awareness session with site personnel on Pfizer requirements and to ensure ongoing compliance with study documentation in accordance with prevailing laws, Good Clinical Practices, and Pfizer standards

 Identify and resolve investigator site issues within required timeframes; align with study team and local country colleagues on corrective and preventative actions to close open issues and to prevent recurrence / persistence of issues

 

Additional Responsibilities:

 A good understanding of the Site Activation requirements and processes within the country/region and be able to learn and potentially implement in more than one (1) country

 May be assigned as Site Activation Partner Point of Contact (PoC) on a study conducted in multi-country

 May be assigned as an SME on a system and/or process, and represent the SAP function as applicable

 May represent the SAP role on global initiatives

 Able to act as an SME on projects and initiatives, as requested

 Support the mentoring of new hires on processes/ systems Systems & Tools Ability to use and learn systems, and to use independently

 Clinical Trial Management Systems (CTMS)

 

 

Education

 School diploma/certificate with equivalent combination of education, training and experience; BS/BA or bachelor’s degree in life sciences preferred

 

Experience

 Minimum 2 years relevant experience in clinical site management.

 Experience working in the pharmaceutical industry/or CRO in study site activation is an asset

 Knowledge of clinical trial methodologies, ICH/GCP, FDA and Global and local country regulations

 Must be fluent in Local language and in English. Multilanguage capability is an asset

 Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization

 Good technical skills and ability to learn and use multiple systems

Please apply in English only

To apply, please visit our website www.pfizercareers.com and search job ID: 4830095


Informace o pozici

Společnost
Pfizer, spol. s r.o.
Address
Stroupežnického 3191/17, Praha – Smíchov
Required education: University
Required languages: Czech (Proficient), English (Advanced)
Listed in: Pharmaceutical
Employment form
Employment form: Full-time work
Employer type: Employer

Pfizer, spol. s r.o., Sara Polvora
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