Total 185 Junior Executive clinical research job vacancies in Others category in Malaysia

Mon Tue Wed Thur Fri am Ward Work Theatre Outpatients OPD Emergency Clinic pm Ward Work Theatre Teaching/Audit OPD (Supernumerary) off

Clinical Coding Assistant/Administrator: To be responsible for the read coding of relevant information into patients electronic healthcare records on SystmOne clinical system, adhering to the Correspondence Management Policy. Process incoming emails into the practice generic email read coding to patient electronic record, responding to patients and external stakeholders. Provide administrative support to the senior management team (operations & practice managers). In addition, the post holder will support the multi-disciplinary team, providing administrative support as required, in line with the needs of the organisation. The following are the core responsibilities of the clinical coder. There may be, on occasion, a requirement to carry out other tasks. This will be dependent upon factors such as workload and staffing levels. a. Accurately clinically coding data on SystmOne into the patient record. b. Identifying relevant clinical information documented in patient correspondence, coding appropriately and completing any detailed action. c. Inputting and extracting data as required to support practice reports. d. Filing and storing records as required. e. Photocopying documentation as required. f. Actioning all incoming correspondence, emails and mail in a timely manner. g. Scanning patient related documentation and attaching scanned documents to patients healthcare records. h. Inputting data into patients healthcare records as necessary. i. Summarising new patients medical records. j. Processing new patient registrations. k. Carrying out system searches as requested. l. Maintaining a clean, tidy, effective working area at all times. m. Supporting all clinical staff with general administrative tasks as requested. Secondary Responsibilities: In addition to the primary responsibilities, the clinical coder may be requested to: a. Review and update the practice coding policy as required (in conjunction with the correspondence manager and practice manager) b. Partake in audit as directed by the audit lead (clinical manager) c. Process patient recalls as part of the practice long term conditions management targets. d. Support reception staff, providing cover during staff absences - Answering incoming telephone calls, transferring calls or dealing with the callers request appropriately, Book appointments e. Complete opening and closing procedures in accordance with the duty rota

Coordinate and improve trial communication throughout Multi-Disciplinary Teams throughout the Trust Maintain effective communication with patients, carers and professional to ensure service delivery Communicates effectively with research team and study participants and their family members. Is able to provide patients with information, which may be complex or sensitive, regarding their participation in the clinical trial and the care that they will receive as a consequence of that Facilitate the recruitment of research participants in to low risk research studies, which is likely to include quality of life and tissue sample collection studies Support the research delivery team to successfully deliver a broad ranging portfolio of clinical trials Coordinate and supervise housekeeping duties and ordering of all clinical trial supplies Co-ordinate the collection transfer and storage of blood / tissue samples in accordance with the Human Tissue Act 2004 as required by trial protocol As a flexible working friendly organisation, we want to be sure that you can work in a way that is best for us and for our patients, and for you. Speak to us about how we might be able to accommodate a flexible working arrangement. If it works for the service, we will do our best to make it work for you. Please note it is a requirement of The Newcastle upon Tyne Hospitals NHS Foundation Trust that all successful candidates who require a DBS for the post they have been offered pay for their DBS certificate.The method of payment is a salary deduction from your first months pay.

Please see detailed Job Description and Person Specification attached for more information regarding this role.

Responsibilities:

• Assist physiotherapists in implementing treatment plans for patients.
• Conduct therapeutic exercises and activities with patients under the supervision of a physiotherapist.
• Provide support in the application of modalities such as heat, cold, ultrasound, and electrical stimulation.
• Guide and educate patients on proper exercise techniques and home care programs.
• Assist in the maintenance and organization of treatment areas and equipment.
• Monitor and record patient progress and report to the supervising physiotherapist.
• Collaborate with other healthcare professionals to ensure comprehensive patient care.
• Adhere to ethical and professional standards in the delivery of physiotherapy services.

Requirements:

• Degree in Physiotherapy or equivalent
• At least 2 – 3 years of experience in a clinical setting with pediatric background.
• Ability to work within short notice.

Interested candidates who wish to apply for the advertised position, please click on the APPLY button below to send in your resume or send to gs1@talenttradersg.com.

EA License No: 13C6305

Reg. No.: R24120209

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

Please view the attached Job Description and Person Specification documents for full details regarding this post. When completing your application please ensure that you clearly demonstrate how you meet the role criteria. This vacancy is advertised on a fixed term contract basis for a period of 15 months due to the post being externally funded. The fixed term contract status of the post holder will be reviewed in accordance with the Trust's legal obligations regarding fixed term contracts taking into consideration the ongoing source of the external funding and the requirement for the post to be maintained. Please also note any secondment must first be agreed with your current line manager.

Duties - Professional To take history, examine and record all findings of all patients admitted under the Consultants care. Carry out and arrange all relevant investigations. To see and examine all patients under the care of the Consultant concerned, including those in the High Dependency Unit. To arrange for the transfer of patients to other hospitals or discharge home, including completion of a discharge summary. To keep the Specialist Registrar and Consultant informed of any changes in their patients condition. To communicate to a patient relative the progress of that patient. To be available for emergency calls to ITU and other parts of the hospital, if required i.e. for cardiac arrest. To participate in research projects which may already be in progress. To participate in lecturing to other staff if required, e.g. nurses and physiotherapists. To accept that occasional emergencies and unforeseen circumstances may occur, and to respond to the needs of the service when they arise.

On-Call There is no on-call attached to this post. Clinical Assessment and treatment of patients according to the British Association of Sexual Health (BASHH) and British HIV Association (BHIVA) guidelines and local/directorate protocols. Research/Audit The post holder will be encouraged to involve themselves in local research/audit. Administrative Assist Medical Staff in diagnosing, coding and review of positive results. The Sexual Health and HIV services in Hertfordshire are a joint initiative between CWFT and Central London Community NHS Trust (CLCH), with CWFT providing the HIV care and CLCH providing Sexual Health care. The service consists of three integrated level three sexual health hubs; Watford clinic, Southgate Clinic in Stevenage, and Hatfield Clinic. All three locations have recently refurbished facilities. There are an additional two nurse-led level two sexual health clinics in Borehamwood and Cheshunt plus online services for STI testing and routine and emergency contraception. Typical clinical activity within the sexual Health service is approximately 72,000 per annum. There is also an ongoing programme of training in general contraception and contraceptive procedures which is provided by faculty-registered trainers for both internal and external candidates. In addition, we have two ST1 trainees based at the Watford and Hatfield Clinics who are part of a rotational GP VTS training scheme. The HIV outpatient services, delivered by CWFT, are based at Watford and Stevenage, and manage a total cohort of around 1000 patients. There is a close working partnership with the HIV outpatient and inpatient teams at Chelsea & Westminster Hospital, allowing patients with complex needs to be referred to a wide variety of specialist joint clinics, an HIV Day care facility, and a specialist HIV ward. The inpatient team provide advice and support for the Watford and Stevenage HIV teams and to the medical teams at the neighbouring acute hospitals (Watford General Hospital and The Lister Hospital, Stevenage), when needed. CWFT also run an HIV outpatient service for around 260 patients in neighbouring Harlow which is open on Tuesday and Wednesday only.

The post will be integrated into the elective and emergency workload of the department. The successful candidates will work alongside the FY1/2, nurse practitioners, and Middle Grade and Consultant teams covering elective and emergencies in the surgical department. Successful candidates will have full support from their teams and supervisors so they can gain the appropriate experience and knowledge in elective and emergency surgery and progress into the next step of their careers. This will include access to clinics, theatre, on calls and ward rounds in both elective and emergency settings. The full educational programme will be discussed and adjusted at the beginning of the placement to meet the post takers training needs. Educational supervision will be available and study leave provided to support the development of your career.

• Position: Clinical Trial Coordinator (Junior Med)
• Salary Range: $2100 to $2400
• Vacancy: 1
• Work Schedule: 5 days a week, office hours
• Location: walking distance from Novena MRT
• Requirements:Diploma qualification
  

Roles & Responsibilities:

1. Develop enrolment/follow-up mechanisms for clinical trials.
2. Enrol and follow up on study subjects.
3. Implement subject follow-up procedures.
4. Complete case report forms (CRF) and maintain study documentation.
5. Monitor and report adverse events.
6. Manage regulatory documents related to clinical trials.
7. Perform any other ad-hoc duties as assigned by the Supervisor.

How to Apply:
send your resume and indicate role(s) you want to apply to: jocelynchan@recruitexpress.com.sg or telegram @jocelynchan

Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience)
Company EA Licence number : 99C4599
Personnel EA License: R1331820

• Working hour: 10am - 9pm (5 days)
• Attractive remuneration package commensurate with relevant experience.

Job Description:

• Provide excellent and friendly frontline customer service
• Attend to enquiry via phone calls
• Schedule patient’s appointment
• Process invoice and payment collections
• Dispense medication and maintaining inventory levels
• Basic housekeeping to maintain the cleanliness of the clinic
• Handle enquiries on promotions and leading customers to products
• To perform other duties as assigned

Job Requirements：

• At least Secondary School / "O" level or equivalent
• Basic IT knowledge
• Pleasant personality, cooperative and work well with co-workers
• Be open to learning new things
• Self-motivated and sales driven with a positive attitude
• Proficiency both in Chinese and strong command in English is a must, who is able to handle Mandarin-speaking customers
• Willing to work retail hours, weekends & public holidays

Work Location: Multiple locations across Singapore!

Interested candidates, kindly submit your updated resume. Alternatively, you may whatsapp our Human Resource Department at 6884 4772.

*We regret that only shortlisted candidates will be notified.

Job description

• Manage the day to day work of dental clinic
• Chair-side assistance of the dentist
• Sterilization of Equipment
• Answering patient enquiries
• Preparing patient for surgeries
• Making appointments and clinic management

Job Requirements:

• Singaporeans only
• Minimum 2 years experience in Dental Clinic
• Relevant experience preferred
• 5.5 day work week, 1.5 off for weekday

Check Aber Care Website for more details.

Interested applicants may email your updated resume to career@abercare.sg.

Abercare.sg | EA License No. 18C9070 | KOH SU WEN, CLARISSA| Registration No. R24119504

Responsible for the admission, clerking and day to day care of their patients on the General Medical wards, as assigned. Participate in the on-call rota. Participate in audits and current research projects. These are available through individual Consultants. Attend the active postgraduate programme with weekly lectures, radiology, medical and pathology meetings, and medical unit presentations. Participate in the teaching of Foundation Doctors at the bedside as well as to Medical Students. Attend practical procedure training. Involvement in Quality improvement projects. To maintain a good working relationship with existing staff members in the hospital. To perform duties in occasional emergencies and unforeseen circumstances at the request of the appropriate Consultant in conjunction, where practicable, with their colleagues both senior and junior.

You will be required to sort specimens sent to the laboratory, key the test orders into the computer system, answer phone calls pertaining to laboratory enquiries as well as attend to walk in patients/visitors. Other job duties may include drawing blood from mostly paediatric patients (fingerprick technique, training will be provided). If you are interested in working in a healthcare environment and have the following requirements, this is the job for you.

Requirements:

• GCE N / O Level, NITEC in Biomedical Science / Nursing
• Equipped with phlebotomy skills advantageous
• Minimum typing speed of 35 wpm
• Will be required to work on weekends and Public Holidays (based on roster)
• Prior job experience in a similar setting and familiarity with terminology used in the Laboratory would be an advantage

DUTIES AND RESPONSIBILITIES The specific responsibilities will depend on the requirements of each team, but may include Act as a point of contact for the Research and Development core team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to general trial conduct Assist with the general administrative duties associated with the set up and initiation of rials within an assigned team, under the supervision of the Senior Clinical Trials Coordinators Assist with completion of activity logs to enable invoices to be raised. Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times Assist with the processing of trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines, under the supervision of the Senior Clinical Trials Coordinators Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety reporting in accordance with protocol requirements, under the supervision of the Senior Clinical Trials Coordinators Complete team reporting mechanisms (i.e. recruitment activity logs, patient visit logs, costing spreadsheets, case report form trackers and electronic proformas) Assist the Clinical Trials Coordinators with the development of trial workbooks for review by the lead Clinical Research Nurse and Principal Investigator Ensure collection of clinical case notes for all patients, so that these are available as needed, for monitoring and audit purposes. Complete case report forms as per sponsor requirements, and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits. This will be under the supervision of the Senior Clinical Trials Coordinators Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature. Arrange shipping and delivery of relevant trial data and documents including import/export of tumour blocks, ECGs and copy scans Arrange team and trial related meetings as required, producing minutes in a timely manner Ensure that data is available and up to date for any meetings related to a clinical trial in collaboration with the Senior Clinical Trials Coordinators Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) Assist with general preparation for audit and inspections within assigned teams, under the direct supervision of the Senior Clinical Trials Coordinators and lead Clinical Research Nurse Assist with trial document archiving by following the Trusts archiving guidelines Ensure that office/ trial related supplies are adequate and assist with the ordering process Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment teams. Demonstrates the agreed set of values and accountable for own attitude and behaviour.