Study Personnel

2 weeks ago

Bengaluru, India Syngene Full time
Job description
Job title: Research Associate
Job location: Bangalore
Job grade: 9-I
At syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit
Mandatory expectation for all roles as per Syngene safety guidelines
Overall adherence to safe practices and procedures of oneself and the teams aligned
Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards
Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
Compliance to Syngene’s quality standards at all times
Hold self and their teams accountable for the achievement of safety goals
Govern and Review safety metrics from time to time
Core Purpose of the Role:
As a Study Personnel - Genetic Toxicology:
Responsible for assisting in Genetic toxicology (Bacterial reverse mutation test, In vitro Chromosomal aberration, and micronucleus test; In vivo Chromosomal aberration and micronucleus test) studies are carried out to the required scientific and regulatory standard and review and approve the study data.
You will be familiar with conducting all work in compliance with applicable regulatory requirements governing the work in which they are involved, such as GLP.
Role Accountabilities:
• Assist in conduct of study in compliance with the Principles of Good Laboratory Practice.
• Comply with the instructions given in the study plan and appropriate Standard Operating Procedures applicable to their involvement in the study. Any deviation from these instructions should be documented and communicated directly to the Study Director, and/or if appropriate, the Principal Investigator(s).
• Record raw data promptly and accurately and in compliance with Principles of Good Laboratory Practice and ensure the quality of their data.
• Exercise health precautions to minimize risk to them and to ensure the integrity of the study. Communicate to the appropriate person any relevant known health or medical condition in order that they can be excluded from operations that may affect the study.
• Sampling (Quarantine, Sentinel, feed, Air sampling, Monthly monitoring rooms and water) and analyzed on timely basis.
Syngene Values
All employees will consistently demonstrate alignment with our core values
Excellence
Integrity
Professionalism
Specific requirements for this role
Experience
0 to 3 years
Skills and Capabilities:
• You should have good understanding and hands on Experience of Genetic toxicology. Preferably have knowledge of related disciplines, slide reading, cell culture handling and microbial counting.
• Ideally, you should be working in, or have Experience within contract research, pharmaceutical companies or have an academic background related to a toxicology discipline.
Education
To be successful in this position, you will need to hold a degree or above in a life sciences discipline (B.Sc./ M.Sc./ B.V.Sc./ M.V. Sc / M. Pharm).

  • Centralized Study Associate I

    23 hours ago

    Bengaluru, India Labcorp Full time

    Position provides process, control, coordination, and approval of clinical trial documents. Position is responsible for ECD, Phase I-IV electronic trial master file (eTMF). ¨ Maintains an understanding of applicable regulatory requirements. ¨ Managing electronic Trial Master Files (eTMF), (Trial, Country and Site artifacts) for clinical studies in...

  • Ssua- I

    3 days ago

    Bengaluru, Karnataka, India ICON Full time

    At 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,...

  • Ssua- I

    3 days ago

    Bengaluru, Karnataka, India ICON plc Full time

    At 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,...

  • Executive Director, Non-Interventional Study Planning

    5 days ago

    Bengaluru, India 1054 GlaxoSmithKline Services Unlimited Full time

    At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people over the next 10 years. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong...

  • Senior Research Scientist

    2 days ago

    Bengaluru, India Syngene Full time

    Job description Job Role: Study Director - Toxicology  Job title: Research Scientist Job location: Bangalore Job grade: 7-I At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety...

  • Senior Research Scientist

    4 weeks ago

    Bengaluru, India Syngene Full time

    Job description Job Role: Study Director - Toxicology  Job title: Senior Research Scientist Job location: Bangalore Job grade: 7-II At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following...

  • Test Report

    1 month ago

    Bengaluru, India Larsen & Toubro Infotech Limited Full time

    Actively involved in the entire business process study relating to SAP HCM day to day production incidents, change requests, enhancements and new developments. - Actively involved in the entire configuration of Payroll, Time Management, Personnel Administration and Organizational Management and ESS/MSS Involved in all phases of support process like...

  • Clinicalinvestigator,clinop-arpl-bc Ar

    2 months ago

    Bengaluru, India Apotex Research Private Limited Full time

    **About Apotex Inc.** **Job Summary**: Handle and administer the BE studies or clinical trial in Bioequivalence center, India also managing the screening and in study assessment and medical care of clinical volunteers. **Responsibilities**: - Conducts duties following established Apotex Research Pvt. Ltd., Bioequivalence Center’s Standard Operating...

  • Safety Science Coordinator

    4 weeks ago

    Bengaluru, India Labcorp Full time

    Assist in the processing of expedited safety reports (ESRs). This includes, but is not limited to: - maintenance of adverse event tracking systems - set-up and maintenance of project files, core process files and central safety files - reporting of ESRs to clients, regulatory authorities, ethics committees, investigators and Labcorp project personnel, if...

  • Sterility Assurance Laboratory Manager

    2 months ago

    Bengaluru, India Baxter Full time

    Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney...

  • Statistical Programmer

    10 hours ago

    Bengaluru, India Integrated Personnel Services Limited Full time

    Role: Clinical Statistical ProgrammerLocation: Bangalore, Noida, HyderabadShift: GeneralJob Description: We are looking for an associate with at least 5+ years of experience for Sr Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards.Associate should be able to...

  • Statistical Programmer

    1 day ago

    Bengaluru, India Integrated Personnel Services Limited Full time

    ole: Clinical Statistical ProgrammerLocation: Bangalore, Noida, HyderabadShift: GeneralJob Description: We are looking for an associate with at least 5+ years of experience for Sr Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards.Associate should be able to...

  • Statistical Programmer

    2 days ago

    Bengaluru, India Integrated Personnel Services Limited Full time

    ole: Clinical Statistical ProgrammerLocation: Bangalore, Noida, HyderabadShift: GeneralJob Description: We are looking for an associate with at least 5+ years of experience for Sr Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards.Associate should be able to...

  • Statistical Programmer

    8 hours ago

    Bengaluru, India Integrated Personnel Services Limited Full time

    Role: Clinical Statistical ProgrammerLocation: Bangalore, Noida, HyderabadShift: GeneralJob Description: We are looking for an associate with at least 5+ years of experience for Sr Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards.Associate should be able to...

  • Tmf Reviewer Ii

    3 days ago

    Bengaluru, India Fortrea Full time

    Position provides process, control, coordination, and approval of clinical trial documents. Position is responsible for ECD, Phase I-IV electronic trial master file (eTMF). - Maintains an understanding of applicable regulatory requirements. - Managing electronic Trial Master Files (eTMF), (Trial, Country and Site artifacts) for clinical studies in accordance...

  • Biostatistician

    4 weeks ago

    Bengaluru, India Lilly Full time

    At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our...

  • Sr Analyst I Controllership

    1 day ago

    Bengaluru, India INET EIT Services India P. Ltd [Formerly Hewlett Packard Global Soft India P.Ltd] Full time

    Job Description: Essential Job Functions Prepares and posts more complex journal entries for company accounts ensuring information is accurate and up to date. Reconciles balance sheet and income statement accounts to general ledger; researches more complex discrepancies and determines appropriate course of action. Prepare complex bank...

  • Biostatistician

    1 month ago

    Bengaluru, India Lilly Full time

    We’re looking for people who are determined to make life better for people around the world.Purpose:The Clinical Project Statistician develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, veterinarians, and/or medical colleagues.The Clinical Project Statistician is responsible...

  • Programmer Iii

    3 days ago

    Bengaluru, India Quanticate Full time

    This is an excellent opportunity for junior programmers who want to make a jump to a higher role, and to develop mentorship skills. You will get opportunity to work on end-to-end studies starting from creating SDTM/ ADAM datasets, writing specifications and generating TLFs. You will also get opportunity to mentor junior programmers within the assigned...

  • Counselor

    1 month ago

    Bengaluru, India Uniglobe Consultants Pvt Ltd Full time

    Job Role - Counselor/ Admission Officer Industry Type - Abroad Education. Job Brief **Roles and Responsibilities** - To Counsel the students/ parents regarding study abroad options. - To handle enquiries and getting the enrollments done. - To do Telephonic Counseling. - To create the networking with students for career counseling, generating leads and...