Manager (Clinical Trial - Contracts)

Singapore Health Services Pte LtdManager, Clinical Trial Coordinating Centre (Contract):Job Category: Administration- Posting Date: 3 Apr 2024The Clinical Trials Coordinating Centre (CTCC) is SingHealth's overarching infrastructure for clinical trials and clinical research. With an oversight of the clinical trials and research operational activities...

Singapore Health Services Pte LtdSenior / Executive, Clinical Trial Coordinating Centre (Contract):Job Category: Administration- Posting Date: 3 Apr 2024The Clinical Trials Coordinating Centre (CTCC) is SingHealth's overarching infrastructure for clinical trials and clinical research. With an oversight of the clinical trials and research operational...

Roles & ResponsibilitiesOur global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Site Contracts team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous...

Job Details:LocationSingaporeSalaryCompetitive SalaryJob TypePermanentRefBH-19255ContactRoselle Cuntapay- Postedabout 1 hour ago We are currently looking for a Clinical Trials Associate for an oncology focused ADC business. They are relatively new to Asia and have been ramping up their clinical presence across the region and are looking for somebody to...

Job Req ID: 1131- Location: Singapore, SGP, SGP- Additional Locations: N/A- Department: Early Stage Development- Job Type: Full Time- Workplace Type: HybridClinical Trials Associate:Company DescriptionWhy Work With UsNothing is more critical to our success than the quality of our team. The work we do is meaningful and impactful - we care about each other as...

Roles & ResponsibilitiesThe Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials...

**Job Overview: Key Responsibilities: Serve as the unblinded point of contact for logistics vendors and unblinded CRAs. Generate and review shipment documents, including batch records, Certificate of Conformance (CoRC), temperature logger data, etc. Manage investigational product (IP) inventory and ensure proper storage and distribution. File unblinded Trial...

Career CategoryClinicalJob Description:HOW MIGHT YOU DEFY IMAGINATION?Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics but...

(Senior) Contracts SpecialistLocation: SingaporeAs a Contracts Specialist or as a Senior Contracts Specialist you will play a key role in improving the lives of patients by accelerating the development of our customers' drugs and devices through innovative solutions.You will be partnering with one of the worlds premier Biopharmaceutical companies. Working...

Roles & ResponsibilitiesAbout TUMCREATETUMCREATE is a multidisciplinary research platform of the Technical University of Munich (TUM) at the Singapore Campus for Research Excellence and Technological Enterprise (CREATE). We are joining forces with universities, public agencies, and industry for the advancement of future technologies.Please visit...

Roles & ResponsibilitiesAbout TUMCREATETUMCREATE is a multidisciplinary research platform of the Technical University of Munich (TUM) at the Singapore Campus for Research Excellence and Technological Enterprise (CREATE). We are joining forces with universities, public agencies, and industry for the advancement of future technologies.Please visit...

Responsibilities: Assist Clinical Team with accurately maintaining clinical trials documents (E.g TMF) for various projects including preparation, handling, distribution, filing of clinical documentation and periodic review and QC check of study files for accuracy, completeness and audit readiness. Assist Clinical Team in liaison with external vendors, track...

Job responsibilities: Manage the whole process for clinical site contracts including contracts and amendments preparation, negotiation, escalation, translation, sending and signature Be Responsible/pointofcontact for the contracting process for both inhouse and locally outsourced studies Escalate contract and budget issues to Legal or Pricing Group and local...

Job responsibilities: Manage the whole process for clinical site contracts including contracts and amendments preparation, negotiation, escalation, translation, sending and signature Be Responsible/pointofcontact for the contracting process for both inhouse and locally outsourced studies Escalate contract and budget issues to Legal or Pricing Group and local...

Roles & ResponsibilitiesJob Purpose A clinical research coordinator will assist Principal Investigator or Co-investigators to monitor the administration and progress of a clinical trial.Duties and ResponsibilitiesPrimary Duties and ResponsibilitiesClinical Trial Oversee overall clinical operations related to the conduct of the clinical trials. To adhere...

Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services...

Roles & ResponsibilitiesResponsibilities: Provide research support service for clinical trials/research in accordance to ICH-GCP and protocol requirements Independently responsible for administration of clinical trials as assigned by Principal Investigator (PI) at his/her professional discretion Assist the sponsor or PI in the submission process for CIRB...

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and...

Clinical Trial Coordinator(1-year)Location: NovenaSalary: 2200 - 2700Office hours Monday to Friday Roles & Responsibilities Develop enrolment/follow-up mechanisms Enrolment and follow-up of study subjects Subject follow-up procedures Case report form (CRF) completion and study documentation Adverse event monitoring and reporting responsibilities Regulatory...

Clinical Trial Assistant (1-year)Location: NovenaSalary: 2200 - 2700Office hours Monday to Friday Roles & Responsibilities Develop enrolment/follow-up mechanisms Enrolment and follow-up of study subjects Subject follow-up procedures Case report form (CRF) completion and study documentation Adverse event monitoring and reporting responsibilities Regulatory...