Remote Site Medical jobs

Our Regulatory Affairs team boasts practical knowledge in the North American and International regulatory arenas through all phases of the drug-development process. We hold extensive industry experience shaping project plans to meet diverse regulatory requirements. Our experts strategize the most efficient route for our clients’ products, from bioanalytical study requirements, pre-IND/pre-NDA meetings with the FDA, and applications to Competent Authorities and Ethics Committees, to successful marketing applications, while providing the necessary guidance to ensure continual regulatory compliance.

What you will do

• Liaise with SAR colleagues to drive plan, organize, compile, progress, track, and submit regulatory submissions on a timely basis and with a consistently high level of quality.

• May act as a contact point for translation review of submission documents such as applications, synopses, ICFs, labels, etc.

• Maintain country-specific patient information sheet and consent form customization text, Maintain country-specific drug labeling information and Country Intelligence Pages

• Review and make recommendations on all relevant documentation e.g. labels, patient information sheets, diary cards etc. to comply with ICH GCP & country-specific requirements.

What you will bring to the role

• Organizational and time management skills

• Aptitude for planning, strategizing, managing, monitoring, scheduling, and critiquing skills

• Strong written and verbal communication skills to clearly and concisely present information in English and local language both

• Strong ability to handle multiple tasks in a fast-paced and changing environment

• Proficiency in MS Office applications, including Microsoft Word, Excel, and PowerPoint

• Strong understanding of country-level cultural norms and local healthcare systems; ability to initiate and develop relationships with local investigators and key site personnel.

Your experience

• A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy, or other related sciences

• Minimum three years of experience in clinical research, preferably in site activation and/or regulatory-related function

• Previous experience within the pharmaceutical/CRO industry.

• Thorough knowledge of ICH GCP, EU Clinical Trials Directive, and other relevant guidance on conducting clinical research.

• Experience in regulatory submissions in Australia

• Multilingualism preferred; working knowledge of English.