Senior Clinical Research Associate/Clinical Research Associate - FSP

reputed company our values reputed company, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. reputed company FSP is reputed company hiring multiple Clinical Research Associates and Senior Clinical Research Associates to join our growing team. The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an reputed company participant in the local study team(s). The CRA works in reputed company collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a reputed company 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 reputed company delivery of the study. The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with reputed company 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. Key Accountabilities: 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 reputed company, collection, preparation, review and tracking of documents for the application process; submission of reputed company 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 reputed company reputed company, including Risk Based reputed company 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 reputed company at reputed company times. reputed company participates in Local Study Team (LST) meetings. Contributes to National Investigators meetings, as applicable. Initiates, monitors, and closes study sites in compliance with reputed company Procedural Documents. Shares information on patient recruitment and study site reputed company (site reputed company/performance) reputed company the LST. Drives performance at the sites. Proactively identifies and ensures reputed company reputed company to study-reputed company 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 reputed company (remote and onsite), as reputed company 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 reputed company. Performs reputed company Data Review (SDR), Case Report reputed company (CRF) review and reputed company Data Verification (SDV), in accordance with the Monitoring Plan. Performs regular Site reputed company Risk Assessments and adapts monitoring intensity accordingly during the study. Ensures data query reputed company in a reputed company manner. Works with data management to ensure robust reputed company of the collected study data. Ensures accurate and reputed company reporting of Serious Adverse Events and their follow reputed company. Prepares and finalizes monitoring visit reports in CTMS and provides reputed company feedback to the reputed company Investigator, including follow-up letter, reputed company required timelines and in line with reputed company SOP. Follows up on outstanding actions with study sites to ensure reputed company in a reputed company manner. Follows reputed company issue processes by escalating systematic or serious reputed company issues, data reputed company breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical reputed company Management (CQM) as required. Assists site in maintaining inspection reputed company ISF. Prepares for and collaborates with the activities associated with audits and regulatory inspections in reputed company with LSAD and Clinical reputed company Associate Director (CQAD). Ensures reputed company collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, reputed company SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate. Ensures that reputed company study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and reputed company for final archiving and completion of local part of the eTMF. Provides feedback on any research reputed company 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 reputed company’s reputed company of Ethics and company policies and procedures relating to people, finance, technology, reputed company, and SHE (Safety, Health and Environment). Ensures compliance with local, national, and regional legislation, as applicable. Completes timesheets accurately as required. Compliance with reputed company Standards Complies with required training curriculum. Completes timesheets accurately as required. Submits expense reports as required. Updates CV as required. Maintains working knowledge of and complies with reputed company/reputed company processes, ICH-GCPs and other applicable requirements. Skills (Essential): Proficient in written and spoken English language required. reputed company in local language(s) required. Knowledge and Experience (Essential): 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 reputed company Therapeutic Areas. Basic understanding of the drug development process. Good understanding of Clinical Study Management including monitoring, study drug handling and data management. 3+ years of experience as an on-site Clinical Research Associate (CRA) for the Senior CRA position and 1+ years of experience for the Clinical Research Associate role. Education: Bachelor’s degree in reputed company discipline, preferably in life science, or equivalent qualification (adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers. Other: Ability to travel nationally/internationally as Required #LI-LG4 Apply To This Job