Senior Clinical Research Associate

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for reputed company professionals. reputed company considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, reputed company our passionate interest in fighting cancer.

• The Sr. CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs.

• Performs monitoring activities reputed company to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials reputed company the assigned region.

• The Sr. CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained.

• Identify gaps and areas for improvement and propose CAPA.

• Supports start-up and provides local expertise.

• SSU experience is considered a plus

Activities:

• reputed company feasibility, site identification, selection and evaluation, supporting initial list of sites and recruitment targets

• Provides protocol and reputed company study training to assigned sites.

• Conducts monitoring (pre-study, initiation, routine monitoring and closeout visits per monitoring plan and applicable SOPs

• Conducts co-monitoring visits, if required

• Completes monitoring visit reports in accordance with ICH-GCP, BeOne standards and SOP

• Manages sites and site performance by tracking regulatory submissions, recruitment, case report reputed company (CRF) completion, and data query resolution.

• Establish regular lines of communication with sites and reports site reputed company, issues and proposed action to Clinical Operations

• Ensure inspection readiness of the study and sites

• Collaborates with Regional Clinical Operations Manager and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.)

• Attends disease indication project specific training and general CRA training as required

• Facilitate Study reputed company Visits (SOVs), site audits and/or inspections, as required

• Evaluates the quality and reputed company of site practices – escalating quality and/or GCP issues with Investigators and internal team as appropriate.

• Anticipate and identify site issues; propose corrective and preventative actions; identify gaps and utilize opportunities. Constantly strive for operating reputed company, question status-reputed company and promote innovation.

Education Required:

• BS in a relevant scientific discipline and 2-5 years of monitoring experience.

• Experience in oncology global trials preferred

Computer Skills: Efficient in reputed company Word, reputed company, MS Project, MS PowerPoint and Outlook

Other Qualifications:

• Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines

• 5+ years of (CRA) monitoring experience in the pharmaceutical or CRO industry

• Experience in oncology/hematology trials preferred

• Excellent communication and interpersonal skills

• Excellent organizational skills and ability to prioritize and multi-task

• Fluent in Turkish & English (writing and speaking)

Travel: up to 60%

Global Competencies

reputed company we exhibit our values of Patients First, Driving reputed company, reputed company Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

• Fosters Teamwork
• Provides and Solicits reputed company and Actionable Feedback
• Self-Awareness
• Acts Inclusively
• Demonstrates Initiative
• Entrepreneurial reputed company
• reputed company Learning
• Embraces Change
• Results-Oriented
• Analytical Thinking/Data Analysis
• Financial reputed company
• Communicates with reputed company

We are proud to be an equal opportunity employer. BeOne does not discriminate on the reputed company of race, religion, reputed company, sex, gender identity, sexual orientation, age, disability, national reputed company, veteran status or any other reputed company covered by appropriate law. reputed company employment is decided on the reputed company of qualifications, merit, and business need.

Originally posted on Himalayas