insurance brokerage in Bedfordview is looking for an Internal Recruitment Consultant to join the team. The successful ensuring successful placements that align with our internal needs. Strategic Planning: Collaborate with management regular communication and a deep understanding of internal business goals. Candidate Sourcing and Assessment:
insurance brokerage in Bedfordview is looking for an Internal Recruitment Consultant to join the team. The successful ensuring successful placements that align with our internal needs. Strategic Planning: Collaborate with management regular communication and a deep understanding of internal business goals. Candidate Sourcing and Assessment:
Applications are invited for the position of Senior IT Internal Auditor (Peromnes Grade 6) based at Head Office organisation's risk management, governance, and internal control processes are operating effectively, and and Preparation - Develop the three-year rolling internal audit strategy and annual Audit Plan. Plan and the approved internal audit plan . Plan, execute and monitor the execution of the internal audit projects methodologies. Manage the project team and co-sourced internal audit service providers and their performance
level? Looking for an opportunity to work the International Market? Do you previous recruitment or sales
level? Looking for an opportunity to work the International Market? Do you previous recruitment or sales
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Desirable
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement programme
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control