Clinical Research Associate

**Parexel FSP** is looking for Oncology Experienced CRAs in **Chile**, **Argentina**and **Peru**

**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 Client 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.

**Responsibilities**:
**Site Management Responsibilities**

- Contributes to the selection of potential investigators.
- In some countries, as required, CRAs are accountable for study start-up and

regulatory maintenance. Tasks may include Site Qualification Visits,
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

training 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.
- Initiates, monitors, and closes study sites in compliance with Client

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 ensures timely

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 (Investigator Site File (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 finalizes monitoring visit reports in CTMS and provides timely

feedback to the Principal Investigator, including follow-up letter, within
required timelines and in line with Client 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, Clinical Study Protocol (CSP) or ICH-GCP
compliance issues to Local Management and/or Clinical Quality
Management (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 Clinical Quality Associate
Director (CQAD).

- Ensures timely collection/uploading of essential documents into the eTMF in

accordance with ICH-GCP, Client 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.

- Collaborates with local Medical Science Liaisons (MSLs) as directed by

LSAD or line manager.

**Compliance with Sponsor Standards**

- Ensures compliance with the Client’s Code of Ethics and 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.

- Completes timesheets accurately as required

**Compliance with Parexel Standards**

- Compli