
Associate Study Coordinator
1 week ago
**1. Protocol Familiarization**: Learn to read and comprehend study protocols, sample analysis outlines, amendments, and study schedules, ensuring understanding of regulatory requirements and Labcorp SOPs/P&Ps relevant to client deliverables.
**2. Data Analysis and Reporting**: Performs initial review of bioanalytical data and originates noncompartmental analysis (NCA) Phoenix WinNonlin in support of pharmacokinetic and toxicokinetic studies. Aids in report preparation, including tables and figures. Compiles analytical information from laboratory groups as required.
**3. Documentation**: Develop skills in preparing and proofing required paperwork for document and/or supply shipments, ensuring timely, efficient, and error-free processing.
**4. Study Phase Scheduling**: Assist in scheduling study phases in coordination with the Study Director/Principal Investigator, Schedulers and Lab Operations.
**5. Quality Checking**: Learn and successfully perform data, and report QC. Assist in checking protocols, proofing tables and figures prepared by others, ensuring proficiency with data collection systems and preparation software.
**6. Coordination with Team**: Work closely with other Study Coordinators (SCs) and Analytical Coordinators (ACs), Document Coordinators (DCs) to assist in preparing, monitoring, maintaining, and understanding finalization/archival, scheduling mechanisms for studies.
**7. Study Archival**: Perform tasks related to study archival, including notifying necessary personnel of study finalization/archival and gathering required paper/electronic items for archival purposes.
**8. Other Duties**: Undertake additional responsibilities as assigned by management.
**Requirements**:
- Master's degree in a related field with 2-3 years relevant experience.
- Strong attention to detail and organizational skills.
- Ability to learn and adapt quickly to new processes and procedures.
- Excellent communication skills, both written and verbal.
- Ability to work collaboratively in a team environment.
- Prior experience in a laboratory or research setting preferred, but not required.
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp 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.
-
Study Coordinator
1 week ago
Bengaluru, Karnataka, India Labcorp Full time**1. Data Analysis and Reporting**: Performs initial review of bioanalytical data and originates noncompartmental analysis (NCA) using Phoenix WinNonlin in support of pharmacokinetic and toxicokinetic studies. Aids in report preparation, including tables and figures. **2. Study Conduct**: Serves as the primary contact for communication and interaction with...
-
Study Coordinator- Tka Project
2 days ago
Bengaluru, Karnataka, India St. John's Research Institute Full time**Brief Description about the Project** Group 1 (Test): Participants in group 1 will receive standard of care with protein supplement for 42 days. Group 2 (Control): Receive standard of care for 42 days The study will be conducted over 42 (6 weeks) days and will follow a randomized, open-labeled, controlled study design at a single center. Eligible...
-
Study Delivery Associate
2 days ago
Bengaluru, Karnataka, India GSK Full time**Site Name**: Bengaluru Luxor North Tower **Posted Date**: Sep 9 2024 **VEO Study Delivery Operations** Value Evidence and Outcomes (VEO) delivers evidence that demonstrates the safety and value of our medicines. VEO is an essential contributor to medicines development and commercialization. VEO builds a deep understanding of patient populations, patient,...
-
Study Start Up Associate I
2 days ago
Bengaluru, Karnataka, India ICON Plc Full timeSSUA I, Bangalore, Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Study Start Up Associate I to join our...
-
Central Global Study Associate
6 days ago
Bengaluru, Karnataka, India AstraZeneca Full timeTypical Accountabilities: - Coordinate SD system activities and collection of SD metrics. Facilitate maintenance of study delivery system data and implementation of system enhancements. Develop reporting tools for SD Systems. Maintain an awareness of the external Process and Technology environment to identify opportunities for Study Delivery - Delivers...
-
Study Document Coordinator
5 days ago
Bengaluru, Karnataka, India beBeeCoordination Full time ₹ 1,04,000 - ₹ 1,30,878Job Title: Study Document Coordinator\This role involves coordinating the processing of study documents, ensuring adherence to client and study requirements as well as ICON SOPs/WPs and relevant regulations.\You will be working closely with study teams and other TMF staff to fulfill your responsibilities effectively. This includes completing departmental...
-
Study Start Up Associate Ii
20 hours ago
Bengaluru, Karnataka, India ICON Plc Full timeStudy Start-Up Associate-II ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Study Start Up Associate II to join our...
-
Study Start Up Associate Ii
7 days ago
Bengaluru, Karnataka, India Icon plc Full timeAt ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...
-
Centralized Study Spec I
1 week ago
Bengaluru, Karnataka, India Fortrea Full timeAs 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, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Centralized Study Spec I
47 minutes ago
Bengaluru, Karnataka, India Fortrea Full timeAs 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, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in...