Erin Cox
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Erin Cox
Recruitment Consultant - Life Sciences
I focus on Regulatory affairs, quality assurance, medical affairs including drug safety, clinical research including data management.
The roles I work on include:
Regulatory Affairs Associate/Manager
Quality Assurance Associate/Manager
PV Associate
Clinical Research Associate
Clinical Project Manager
Clinical Trial Manger
Real Work Evidence Manager
Medical Affairs Associate
MSL
Medical Manager
I have a Medical science degree and 5 years of experience working across public and private healthcare sectors which has allowed me to gain a comprehensive understanding of the industry, specific roles, responsibilities, and what makes candidates exceptional in their respective fields. I enjoy attending industry events including MTAA, ARCS and ACTA to stay up to date with industry news and insights. I personally enjoy partnering with start-ups and expanding teams, acting as an extension of their business. Candidate feedback I have received highlights my professionalism, dedication, thoughtful and efficient.
Jobs by Erin Cox.
Senior Clinical Research Scientist
- Sydney
- Great salary and benefits package
Benefits Competitive salary with range of bonus incentives Opportunity to work with innovative technology Opportunities for career progression and development About the company Our client is a growing international company at the forefront of innovative medical technologies. They are dedicated to improving patient outcomes and advancing the standard of care in their field. The company fosters a dynamic, collaborative work environment with a strong focus on research and development. About the opportunity This is an exciting opportunity to join our client's expanding Clinical Research team. You will play a key role in designing and executing clinical studies on products as well as research areas. This position offers the chance to work on groundbreaking research, collaborate with leading medical experts, and contribute to the development of transformative technologies. Duties Develop clinical study protocols based on regulatory standards/guidelines and literature Contribute to publication strategy and drive clinical study design Oversee all aspects of study conduct, including site selection, data collection, and monitoring Analyze study data and prepare comprehensive reports summarizing findings Collaborate with cross-functional teams to incorporate clinical evidence into product development Skills and Experience Degree in a life sciences discipline and knowledge of microbiology Minimum 4 years of experience in clinical research, in a product development setting Proven track record of successfully designing and executing clinical studies, including protocol writing Excellent project management and problem-solving skills Strong communication and interpersonal abilities to effectively liaise with internal and external stakeholders Culture Our client values innovation, collaboration, and a commitment to excellence. They offer a supportive, inclusive work environment that encourages professional growth and recognizes individual contributions. How to Apply Please submit your resume for consideration. For a confidential discussion about the role, contact Erin Cox at ecox@hpgconnect.com
COMBINED EXPERIENCE
At HPG, we pride ourselves on bringing together a diverse group of professionals with extensive backgrounds in the healthcare recruitment industry. Our combined years of experience and specialised knowledge ensure that we deliver unparalleled service to our clients and candidates. By working collaboratively, we harness our collective expertise to meet and exceed your goals and expectations, providing tailored solutions and exceptional support every step of the way. Discover how our unified team effort drives success in every project we undertake.
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