Specimen Manager
2 weeks ago
**JOB PURPOSE**
The specimen management unit is responsible for the day-to-day management of specimen shipments, specimen handling and specimen logging. Specimens are biological samples collected from either humans or animals and are a valuable resource. Specimens are essential to the biomarker and bioanalytical services conducted at Synexa and are vital to allow us to deliver for our customers.
The unit is a key part in study delivery and supports Synexa delivery teams to achieve study milestones and accomplish deliverables, while delivering for our customers and supporting the teams to deliver revenue targets.
**MAIN AREAS OF RESPONSIBILITY**
**General**
- Provide administrative support as required by the laboratory.
- Perform designated duties in an efficient manner and completing tasks timeously.
- Where required, liaise with procurement and study management teams to arrange couriers for shipment of specimens or compounds/reagents and ensures these are in line with project budgets.
**Specimen Management**
**Pre-Specimen Receipt**
- Primary point of contact for external and internal communication related to specimens and Sponsor provided compounds/reagents.
- Confirm timelines for specimen shipments and ensures updated information is visible to the study delivery team via the Odoo planning app.
- Track incoming specimen and Sponsor provided compound/reagent shipments via courier on-line tracking systems and inform the study delivery team regarding any changes in expected timelines or any challenges/issues identified.
- Upon early receipt of shipping manifest for frozen specimens, log specimens and ensure source quality control checks are performed in the study specific sample log sheet, ensuring compliance with quality control method sheets.
- Highlight and resolve any queries related to specimen shipment manifests, requisition forms or equivalent documentation with the relevant CRO and/or Sponsor and ensure the communication is filed (hardcopy and/or electronic) for traceability.
- Ensure up to date sample log sheets are always available for study delivery team usage.
**Specimen Receipt**
- Ensure adherence to safety procedures upon handling of specimens.
- Receive specimens (as required per site), complete required paperwork and ensure sample log sheets are appropriately updated.
- Where required, file (hardcopy and/or electronic) temperature monitoring data provided by courier and share accordingly with CRO and/or Sponsor upon shipment receipt.
- As required, assist with labelling, sorting and storage of specimens and Sponsor provided compounds/reagents.
- Upon receipt of fresh specimens, log specimens in a timely manner within study specific sample log sheets and conduct source quality control checks of paperwork ensuring compliance with relevant study documentation. This is time sensitive and critical to be prioritised to allow the study delivery team to perform required specimen testing.
- Review documentation received alongside specimen shipments and verify accuracy. Ensure the specimens meet GCP standards and document any integrity related issues.
- Escalate and resolve queries timeously and upon completion, file (hardcopy and/or electronic) paperwork appropriately.
- Communicate receipt of samples to relevant study delivery team members as well as externally to CRO and/or Sponsor.
**Specimen Storage**
- Ensure specimens are stored at the correct temperature and storage location is logged in the study specific sample log sheets.
- Alongside relevant laboratory personnel, manage storage location capacity.
- Maintain storage location upkeep by facilitating scheduled sample reconciliations.
- Upon completion of a project, enquire the fate of specimen(s) with the CRO and/or Sponsor and action decision accordingly.
- Based on laboratory requests, retrieve specimens for sample analysis from storage location and following testing, return and store appropriately and update relevant sample log sheets accordingly.
**Specimen Administration**
- Provide support to the delivery of the lab manual alongside the scientific team to outline specimen collection, processing, storage, and shipment instructions to ensure optimal specimen quality for required testing.
- Assess country specific import/export requirements for biological specimens or Sponsor provided compounds/reagents.
**Phlebotomy/Specimen Collection**
- Ensure local regulatory approvals are in place to allow donor sample collection to proceed.
- Ensure process specific documentation are completed as per local regulatory guidelines, approvals, and internal workflows.
- In response to laboratory requests, perform required tasks to arrange specimen collection from in-house donor(s) or external network.
- Per site requirement and capacity, manage consumables for specimen collection and as required, place orders via LIMS to replenish stock.
- Where qualified, support with blood draws and other sample collection techniques, following appropriate tr
-
Clinical Trial Administrator
6 days ago
Cape Town, South Africa TASK Full time**Overall Purpose of the Position**: As a highly organised and detailed-oriented individual, the Clinical Trial Administrator will be responsible for managing the processing and handling of clinical research samples in compliance with relevant policies, procedures and regulatory standards. The role involves coordinating the receiving, processing, storing and...
-
Research Assistant
3 days ago
Cape Town, South Africa The Aurum Institute Full timeYour primary role will be to participate in: **Participant recruitment and enrolment** - Recruit potential participants for the study - Ensure that potential participants are provided with all the study details as described in the Participant Information Sheet. - Administer informed consent - Recruit and schedule appointments for study participants - Assist...
-
Recruiter
3 days ago
Cape Town, South Africa The Aurum Institute Full timeYour primary role will be to participate in: **Participant recruitment and enrolment** - Recruit potential participants for the study - Ensure that potential participants are provided with all the study details as described in the Participant Information Sheet. - Administer informed consent - Recruit and schedule appointments for study participants - Assist...
-
Recruiter
4 days ago
Cape Town, South Africa The Aurum Institute Full time**Purpose of the Role**: The Recruiter is responsible for meeting the study recruitment and retention targets by mapping the catchment areas, identifying potential participants, developing recruitment and retention plans, implementing the plans and providing regular feedback on the progress made. **Job Specification** **Participant recruitment and...
-
Respiratory Clinical Technologist
3 weeks ago
Cape Town, South Africa University of Cape Town Lung Institute Full timeMinimum Requirements : Certificate / Degree / Diploma in Clinical Technology or another medical field 1 - 2 years experience in clinical research on multiple projects Good Clinical Practice Certification (advantageous) Keen interest in Research (particularly Allergy, Immunology and Dermatology) Computer Literacy (proficiency in Microsoft Office and...
-
Respiratory Clinical Technologist
4 weeks ago
Cape Town, South Africa University of Cape Town Lung Institute Full timeMinimum Requirements: Certificate / Degree / Diploma in Clinical Technology or another medical field 1 - 2 years experience in clinical research on multiple projects Good Clinical Practice Certification (advantageous) Keen interest in Research (particularly Allergy, Immunology and Dermatology) Computer Literacy (proficiency in Microsoft Office and electronic...
-
Research Nurse
2 weeks ago
Cape Town, South Africa University Of Cape Town Lung Institute Full timeMinimum Requirements : Certificate / Degree / Diploma in General Nursing 2 - 5 years experience in clinical research on multiple projects Prior working experience in Paediatrics (or baby clinic) Good Clinical Practice Certification (advantageous) Keen interest in Research (particularly Allergy, Immunology and Dermatology) Computer Literacy (proficiency in...
-
Study Coordinator
2 weeks ago
Cape Town, South Africa University of Cape Town Lung Institute Full timeMinimum Requirements Certificate / Degree / Diploma in General Nursing or Clinical Technology or another medical field 2 - 5 years’ experience in clinical research on multiple projects Good Clinical Practice Certification (advantageous) Keen interest in Research (particularly Allergy, Immunology and Dermatology) Computer Literacy (proficiency in Microsoft...
-
Study Coordinator
7 days ago
Cape Town, South Africa University of Cape Town Lung Institute Full timeMinimum Requirements: Certificate / Degree / Diploma in General Nursing or Clinical Technology or another medical field 2 - 5 years experience in clinical research on multiple projects Good Clinical Practice Certification (advantageous) Keen interest in Research (particularly Allergy, Immunology and Dermatology) Computer Literacy (proficiency in Microsoft...
-
Research Nurse
1 week ago
Cape Town, South Africa University of Cape Town Lung Institute Full timeMinimum Requirements: Certificate / Degree / Diploma in General Nursing 2 - 5 years experience in clinical research on multiple projects Prior working experience in Paediatrics (or baby clinic) Good Clinical Practice Certification (advantageous) Keen interest in Research (particularly Allergy, Immunology and Dermatology) Computer Literacy (proficiency in...