
Clinical Trial Principal Investigator
Há 6 dias
Itapecerica da Serra, São Paulo, Brasil
NES FIRCROFT
Tempo inteiro
**Clinical Trial Principal Investigator / Sub-Investigator**- ** Melbourne location**:
- ** Fast growing, young company with a vibrant culture**:
- ** Generous remuneration package & work/life balance**:
- ** Part-time role (2-3 days p/w)**
NES Fircroft is working with a modern and dynamic privately owned Australian clinical research organisation, looking to add an experienced and motivated doctor to work as
**Clinical Trial Sub-Investigator / Clinical Trial Investigator** at their new Melbourne site.
Our client is open to training an experienced doctor who is excited about entering the clinical research space.
**Role**:
You will be part of a fantastic team offering a stimulating clinic environment, including flexibility, patient interaction and overseeing and assisting the team in delivering important clinical trials.
**Responsibilities**:
- Conduct medical research in accordance with government regulations, guidelines, ICH Good Clinical Practice and SOPs
- Lead studies as a Sub-Investigator /Principal Investigator
- Medical oversight of the study participants enrolled in a trial
- Overall oversight of the study, ethics, participants, schedule of events, AEs and data
- Perform study activities as required by the protocol and applicable regulations
- Interpretation of laboratory results, ECG, imaging
- Read and understand the informed consent form, protocol, and investigator's brochure
- Explain the study to participants and obtain signed informed consent
- Follow up and evaluate study participants for the duration of the study
- Work proactively with a broader team of Investigators across multiple sites to develop and implement clinical best practice
- Assist the Site Operations Manager in developing a high performing team culture
**Requirements**:
- Eligibility for AHPRA Medical Practitioner Registration
- MBBS or equivalent degree from a recognised university
- Research Experience
- A positive 'can do' attitude
- Ability to work independently and as part of a team
- Exceptional organisational skills and attention to detail
- Ability to handle multiple tasks and meet deadlines
- Flexible and open to change and excellent problem-solving ability
- Knowledge of and adherence to local regulatory requirements and professional regulations e.g ICH/GCP guidelines, MA Code of Conduct, National Statement
- Full and unrestricted working rights in Australia
**Highly Desirable**:
- Experience in conducting clinical trials or research
- Experience working in commercially sponsored trial settings
With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Infrastructure, Life Sciences, Mining, Automotive and Chemicals sectors worldwide.With more than 100 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.
-
17732-assoc Clin Project Mgr
1 semana atrás
Serra, Brasil Iqvia Tempo inteiro**Responsibilities**: - Associate Clinical Project Manager - IQVIA has an exciting opportunity for an Associate Clinical Project Manager with strong leadership capabilities to join our project management team in - either Australia or Malaysia. - Job Overview - Associate Clinical Project Managers are an integral part of clinical trial delivery, liaising with...