Centralized CTL II
- Employer
- Fortrea
- Location
- Belgrade, Serbia
- Salary
- Competitive
- Start date
- 4 Dec 2024
- Closing date
- 3 Jan 2025
View more categoriesView less categories
- Discipline
- Clinical Research, Clinical Trials Manager / Administrator
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
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Job Details
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development and technology solutions across more than 20 therapeutic areas. With over 18,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
We are seeking an experienced professional to lead central monitoring activities, ensure the quality of clinical trial processes, and proactively manage risk. As a Centralized Clinical Team Lead, you will play a vital role in ensuring compliance, mentoring teams, and delivering data-driven insights that enhance trial outcomes. Key Responsibilities: Review trip reports, identify risks, and communicate trends or safety concerns. Risk review activities at study, site, and regional levels, ensuring proactive risk management. Collaborate with study teams to refine processes, resolve issues, and ensure data-driven decision-making. Provide mentorship and training to team members on monitoring and reporting processes. Support regulatory inspections and ensure inspection readiness. Managing Protocol Deviations and Quality events as per study needs Qualifications: Degree in Life Sciences or related field; advanced qualifications preferred. 8+ years in clinical research, with 2+ years in centralized monitoring or trip report review. Expertise in ICH-GCP guidelines and regulatory compliance. Strong organizational, analytical, and interpersonal skills.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com . Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
We are seeking an experienced professional to lead central monitoring activities, ensure the quality of clinical trial processes, and proactively manage risk. As a Centralized Clinical Team Lead, you will play a vital role in ensuring compliance, mentoring teams, and delivering data-driven insights that enhance trial outcomes. Key Responsibilities: Review trip reports, identify risks, and communicate trends or safety concerns. Risk review activities at study, site, and regional levels, ensuring proactive risk management. Collaborate with study teams to refine processes, resolve issues, and ensure data-driven decision-making. Provide mentorship and training to team members on monitoring and reporting processes. Support regulatory inspections and ensure inspection readiness. Managing Protocol Deviations and Quality events as per study needs Qualifications: Degree in Life Sciences or related field; advanced qualifications preferred. 8+ years in clinical research, with 2+ years in centralized monitoring or trip report review. Expertise in ICH-GCP guidelines and regulatory compliance. Strong organizational, analytical, and interpersonal skills.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com . Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
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