Pharmaceutical Trainer

2 weeks ago

Sydney, Australia Carecone Full time

**Primary Role & Responsibilities**
- Responsible for customizing and delivering training to our global pharmaceutical customers over various domains in the healthcare vertical.
- Deliver full-day classroom-based training sessions or connect online via Virtual training.
- Work with customers, acting as the SME for course material design with the responsibility of customizing and delivering corporate training/training modules as per the requirements.
- Serve as performance coach through consulting, monitoring, and evaluating training results in the work environment and classroom delivery responsibilities.
- Responsible for understanding the profile of attendees, classroom preparation, classroom setup, and evaluating the success of the learning programs and solutions.
- Should have excellent presentation skills and zeal to explain the minute technical details in an easy way to the participants.
- Works with the delivery manager to provide feedback on class delivery and associated resources.
- Ensuring constant learning process to stay abreast in relevant technologies.
- Independently establishes work priorities and direction with mínimal input from other team members and management.

**Technical Expertise**:

- A bachelor's graduate in Pharmaceutical Science with familiarity working on clinical trial master file documentation, data management, clinical operations, and pharmacovigilance.
- Excellent communication and organization skills coupled with thorough knowledge of ICH-GCP and essential documents involved in clinical trials and regulatory regulations.
- Familiarity with systems like Oracle Clinical, OC-RDC, RAVE, Inform
- Knowledge of different software to file documents electronically like right track, GDMS, ELARA, **ELVIS**, etc. would be preferred.

**Professional Experience & Competence**:

- 8 - 10 Years of Sr CRA experience
- 2-3 years of Line Management or Project Management
- Excellent Communication (English)
- Soft skills awareness
- Clarity on ICH-GCP Guidelines, specifically Essential Documents.
- Practical Exposure to the maintenance of Investigator and central file.
- Perform source data verification and reconciliation of adverse events for market research programs.
- Familiarity and/or experience with electronic Trial Master File systems (eTMF).
- Familiarity and/or experience in defect tracking and reporting using Clinical Data Review System & manual tracking
- Ability to convey SOP requirements theoretically and practically
- Industry certifications in technical areas and/or training will be highly appreciated.
- Someone with regulatory background would be an added advantage.

**Non-Technical Competence**
- Innate ability to share information.
- Excellent written and verbal communication skills including good facilitation skills, excellent presentation skills, and engaging presentation style necessary.
- He /She should be a good motivator, with a lot of energy and enthusiasm with a proven ability to learn quickly, multi-task, and work independently as well as part of a team.
- Must be able to stand and lecture long sessions at a stretch.
- Willing to travel exclusively in domestic as well as international sectors.
- Should be open to learning new technologies and cross-domain competence flexibility.

**Job Types**: Full-time, Permanent

Schedule:

- Monday to Friday

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