Trace Recruit is delighted to be working with a global software business, who is recruiting for a Data Migration Specialist, following the implementation of a new payroll software.
Data Migration Specialist (Payroll) - 18 months FTC - £55,000 - £60,000 - East Berkshire (hybrid working)
This is a great opportunity for a period of 18 months to support the migration of multiple aggregated payrolls into the new software.
Hybrid role - office three days a week Monday/Tuesday/Thursday Maidenhead- WFH 2 days a week.
Must have HR experience and have worked as part of a busy HR team.
The job holder will be required to provide a professional and efficient HR administration service and a high-quality telephone and email advice service, together with transactional support service, ensuring consistency of practice and compliance with corporate people, management policies, processes and standards.
If you're currently studying or have recently graduated in Computer Science/IT/Business Computing, this could be the opportunity for you.
An exciting opportunity has arisen to join a world-leading pharmaceutical organisation!
Initially for 12 months, this position is based out of offices in Maidenhead on a hybrid working arrangement of 3 days on site after a qualifying period.
This is an excellent opportunity for an experienced Clincial Trial Regulatory Specialist to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended.
This role has come about due to expansion and an increase in the production of pharmaceutical.
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.
The Role
They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes.
The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials.
Responsible for the management and overall coordination, status reporting and stability of a variety of enterprise wide projects.
Responsible for assembling project plans, teamwork assignments, directing and monitoring work efforts on a daily basis.
Establishes and implement project management processes and methodologies to ensure projects are delivered on time, within budget, adhere to high quality standards and meet customer expectations.
This biotech is looking to strengthen their Regulatory Labelling group by taking on an experienced Regulatory Labelling professional for a contract job based in West London.