Careers at Pharmalys At Pharmalys, we never lose sight of the fact that our people are the greatest asset of our company. We are committed to their professional and personal development and we create a stimulating and rewarding working environment.
Jobs
Senior Clinical Research Associate – London HR101
Job Details
OVERVIEW Pharmalys are looking for a pro-active Senior Clinical Research Associate (SCRA) to join our Clinical Operations department. If you have a bachelor's degree or equivalent in healthcare or scientific discipline, have significant on-site, independent monitoring experience, we want to hear from you.
ESSENTIAL
A Bachelor's degree or equivalent in a health care or other scientific discipline. Significant on-site, independent monitoring experience. Preferably, a minimum of 3 years in a CRA role within the Pharmaceutical or CRO Industries. Management: You will assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects.Leadership: Knowledge of the regulatory framework that surrounds drug development and the clinical trial process.A Bachelor's degree or equivalent in a health care or other scientific discipline. Significant on-site, independent monitoring experience. Preferably, a minimum of 3 years in a CRA role within the Pharmaceutical or CRO Industries. Management: You will assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects.Leadership: Knowledge of the regulatory framework that surrounds drug development and the clinical trial process.RESPONSIBILITIES
Performing site selection, initiation, monitoring, and close-out visits Maintaining all documentation relating to study set-up and monitoring activities e.g., monitoring plans, visit reports, study status trackers Communicating regularly with assigned study sites and the project teamProvide protocol and related study training to allocated sitesBENEFITS
Competitive salary in keeping with pharmaceutical industry standards and will reflect experience 25 days annual leave plus bank holidays (increasing in increments to 30 days after 6 years long service) Your birthday off work and other benefits ADDITIONAL DETAILS
Job Types: Full-time, Permanent Benefits: Company pension, Private medical insurance, Work from home Schedule: 8 hour shift Monday to Friday Experience: Clinical Research Associate within a CRO: 3 years (required) Work authorisation: United Kingdom (required) Work Location: Hybrid Application deadline: 13/01/2023 To apply for this job, kindly fill the form in the section below and quote the application reference in your cover letter.
Community Manager – Senegal HR103
Job Details
OVERVIEW We are looking for a qualified Community manager to join our team. If you are a tech-savvy professional, experienced in social media, PR and promotional events, we would like to meet you. Our ideal candidate has exceptional oral and written communication skills and is able to develop engaging content. You should be a ‘people person’ with great customer service skills and the ability to moderate online and offline conversations with our community. Ultimately, you should be able to act as the face and voice of our brand and manage all community communications.
ESSENTIAL
Set and implement social media and communication campaigns to align with marketing strategies Significant on-site, independent monitoring experience. Preferably, a minimum of 3 years in a CRA role within the Pharmaceutical or CRO Industries. Management: You will assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects.Leadership: Knowledge of the regulatory framework that surrounds drug development and the clinical trial process.A Bachelor's degree or equivalent in a health care or other scientific discipline. Significant on-site, independent monitoring experience. Preferably, a minimum of 3 years in a CRA role within the Pharmaceutical or CRO Industries. Management: You will assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects.Leadership: Knowledge of the regulatory framework that surrounds drug development and the clinical trial process.Leadership: Knowledge of the regulatory framework that surrounds drug development and the clinical trial process.RESPONSIBILITIES
Performing site selection, initiation, monitoring, and close-out visits Maintaining all documentation relating to study set-up and monitoring activities e.g., monitoring plans, visit reports, study status trackers Communicating regularly with assigned study sites and the project teamProvide protocol and related study training to allocated sitesBENEFITS
Competitive salary in keeping with pharmaceutical industry standards and will reflect experience 25 days annual leave plus bank holidays (increasing in increments to 30 days after 6 years long service) Your birthday off work and other benefits ADDITIONAL DETAILS
Job Types: Full-time, Permanent Benefits: Company pension, Private medical insurance, Work from home Schedule: 8 hour shift Monday to Friday Experience: Clinical Research Associate within a CRO: 3 years (required) Work authorisation: United Kingdom (required) Work Location: Hybrid Application deadline: 13/01/2023 To apply for this job, kindly fill the form in the section below and quote the application reference in your cover letter.
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