Bedfordview is looking for an Internal Recruitment Consultant to join the team. The successful candidate will related field. Proven experience as a Recruitment Consultant, with a focus on the insurance industry. In-depth
Bedfordview is looking for an Internal Recruitment Consultant to join the team. The successful candidate will related field. Proven experience as a Recruitment Consultant, with a focus on the insurance industry. In-depth
Are you a talented sales professional or an experienced recruiter looking to take your career to the next level? Looking for an opportunity to work the International Market? Do you previous recruitment or sales experience? Do you thrive in a fast-paced, dynamic environment where your skills and crea
Are you a talented sales professional or an experienced recruiter looking to take your career to the next level? Looking for an opportunity to work the International Market? Do you previous recruitment or sales experience? Do you thrive in a fast-paced, dynamic environment where your skills and crea
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Desirable Apply Online.
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 Please Apply Online. Please take note that the applicants who do not adhere to the above criteria will
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 Please Apply Online. Please take note that the applicants who do not adhere to the above criteria will
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
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