Clinical Research Associate I - FSP (Fixed-Term 9-12 months; Looking for Study Coordinators wit[...]

Parexel; Brasil; Presencial; BRL 120 000 - 180 000; Tempo integral

Resumo da oferta

Parexel is seeking a Study Coordinator/CRA I for a 9- to 12-month assignment in Brazil. Based in São Paulo, Rio de Janeiro, or Porto Alegre, you will monitor oncology studies and serve as primary site contact.

This role requires ICH-GCP knowledge and oncology experience, with potential expansion to LSAD duties for senior candidates. The CRA ensures study conduct, site initiation, monitoring, and regulatory compliance, collaborating with Local Study Teams to achieve study milestones.

Qualificações

• Bachelor's degree in life sciences or related field.
• Excellent knowledge of ICH-GCP and GMP/GDP basics.
• Strong knowledge of local regulations.
• Excellent written and verbal communication skills.
• Ability to travel nationally and internationally.
• Experience in oncology is preferred.

Responsabilidades

• Contributes to investigator site selection.
• Trains and advises investigators and site staff on study-related matters.
• Maintains CTMS and study data per plan and SOPs.
• Performs monitoring visits (remote and onsite) per Monitoring Plan.
• Ensures timely reporting of Serious Adverse Events and follow-ups.
• Collaborates with Local Study Team (LST) and LSAD to meet study commitments.

Conhecimentos

ICH-GCP knowledge

Local regulations knowledge

Medical knowledge

Written and verbal communication

Interpersonal skills

Negotiation skills

Travel readiness

Formação académica

Bachelor's degree in life sciences

Descrição da oferta de emprego

Parexel FSP is looking for Study Coordinators to join our team as CRA I for a temporary 9-12 months assignment. Candidates can be based in São Paulo, Rio de Janeiro and Porto Alegre and must have previous oncology experience.

Job Overview

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study.

The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Sponsor's Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

A CRA with longer tenure and experience may take on additional responsibilities that include additional tasks associated with LSAD.

CRAs might have different internal titles based on the experience level (CRA, Senior CRA). The experience level depends on the years of experience, performance record, level of independence in the role, ability to take on additional tasks or tutor more junior colleagues. The Director, Country Head may assign this internal title after confirmation with Senior Director, Cluster Head or Executive Director, Regional Head).

Typical Accountabilities

• Contributes to the selection of potential investigators.
• In some countries, as required, SrCRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
• Trains, supports and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
• Confirms that site staff have completed and documented the required trainings appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.
• Actively participates in Local Study Team (LST) meetings.
• Contributes to National Investigators meetings, as applicable. Based Quality Management (RbQM) principles.
• Initiates, monitors and closes study sites in compliance with client’s Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST.
• Drives performance at the sites. Proactively identifies and ensurestimely resolution to study-related issues and escalates them as appropriate.
• Updates CTMS and other systems with data from study sites as per required timelines.
• Manages study supplies (ISF, etc), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.
• Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines and discusses with LSAD the correct timing and type of visits.
• Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
• Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
• Ensures data query resolution in a timely manner.
• Works with data management to ensure robust quality of the collected study data.
• Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.
• Prepares and finalises monitoring visit reports in CTMS and provides timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with client’s SOP.
• Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
• Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, CSP or ICH-GCP compliance issues to Local Management and/or CQM as required.
• Assists site in maintaining inspection ready ISF.
• Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and CQAD.
• Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICHGCP, client’s SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate.
• Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc) are available and ready for final archiving and completion of local part of the eTMF.
• Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
• Ensures compliance with client’s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).
• Ensures compliance with local, national and regional legislation, as applicable.
• Collaborates with local MSLs as directed by LSAD or line manager.

Essential

Education, Qualifications, Skills and Experience

• Bachelor degree in related discipline, preferably in life science, or equivalent qualification (*).
• Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
• Good knowledge of relevant local regulations.
• Good medical knowledge and ability to learn relevant client’s Therapeutic Areas.
• Basic understanding of the drug development process.
• Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
• Excellent attention to details.
• Good written and verbal communication skills.
• Good collaboration and interpersonal skills.
• Good negotiation skills.
• Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
• Ability to travel nationally/internationally as required.
• Previous oncology experience is required.
• Advanced/Fluent english skills is required.

Desirable

• Ability to work in an environment of remote collaborators.
• Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.
• Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
• Good analytical and problem-solving skills.
• Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
• Familiar with risk-based monitoring approach including remote monitoring.
• Good cultural awareness.
• Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an eenabled environment.
• Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.

Key stakeholders and relationships

Internal (to client or team)

• LSADs and Local Study Teams
• Line Manager and local SMM LT
• Clinical Quality Associate Director
• Local Medical Teams: MSLs and Medical Affairs
• Global Study Teams
• Global Clinical Solutions functions
• Clinical Data Management
• Regulatory Affairs
• Patient Safety