Preferred Provider for US - Rapid study Start-up – Recruitment
CROMSOURCE was awarded a program of three studies in the US in the respiratory area.
Through our hybrid delivery platform, we utilised a combination of our people, procedures, systems and supporting infrastructure that underpins all of our partnerships.
We made an immediate assessment of available resources in-house and supplemented this with external hires for functions where there were gaps.
The fully dedicated team were 5 Project Managers, 30 CRA’s, 2 Project Coordinators, and 10 Clinical Trial Administrators to join the Clinical Operations Department.
We had to be ready to hire any external team members as soon as the contract was signed which took approximately 8 weeks. The team had to be available for training immediately on award.
This was an organised and focussed operation with the assignment of the existing team and the onboarding of new staff.
We received 1068 candidates, we screened 165 candidates and 91 were interviewed. Finally 56 candidates had an offer and 47 of them accepted positions.
The whole team was then fully operational within 2 weeks from the signature of the contract.
Shared vision was very important and a true partnership with all key internal stakeholders was needed.
Up-front staff planning in all areas was required, with close communication throughout the recruitment and onboarding stages.
Furthermore, in this situation, knowledge of the US recruitment market was key and our expert recruiters worked with the operational teams in a seamless approach to the recruitment piece.
Proactive marketing of jobs on social media for maximum exposure in the candidate market place was very important in finding enough candidates of the right calibre.
Preferred Provider for European Clinical Trial Supply Management
CROMSOURCE has been working under a Master Services Agreement with a large Pharma company in Belgium for many years.
Through TalentSource, we successfully delivered an office-based team of Clinical Trial Supply Management professionals for their European clinical trial services facilities and have an ongoing relationship with them in the status of First Tier Supplier.
The team consists of Associates and Coordinators, giving support to their Material Sourcing, Distribution, Packaging and Quality Departments.
These clinical professionals have strong backgrounds in Supply Chain and Clinical Trial Packaging. Its mission is to import and export to Europe as well as subcontracting the packaging and distribution of drugs for clinical trials worldwide.
Multitasking, setting of priorities, showing flexibility and problem solving are key competences this team need to demonstrate.
The initial set-up of the team was bound by fast timelines and there were up to 25 staff at its peak. We receive ongoing ad-hoc requests to add to the existing team for which external recruitment is required.
Up-front staff planning in all areas is required with close communication throughout the recruitment and onboarding process.
A specific training program was set-up for the sponsor dedicated team covering soft skills and languages.
Annual Governance Meetings and regular operational level meetings are in place to discuss performance.
Preferred Provider for Global FSP
CROMSOURCE was awarded with a Global Master Functional Service Provider for a large Pharma company, which led on to us being selected as TIER 1 supplier through a partnership program throughout Europe and the United States.
This partnership is across multiple functions with regular resourcing requests for Clinical, Regulatory and Biometrics roles, requiring a very fast ramp-up and turnaround. These timelines and other metrics and Service level agreements were agreed and have been entered into our contracts.
A team of Clinical Project Managers, CMC Regulatory Leads, Site Engagement Managers and other clinical functions, operating in the following countries: Belgium, Bulgaria, Croatia, Czech Republic, France, Germany, Hungary, Italy, Moldavia, Romania, Serbia, Slovakia, Spain, Turkey, UK, Ukraine and US.
The requirements are for the first CVs to be submitted to the client with a maximum of 5 business days and the hit rate (candidates interviewed that are hired) >30%. The average time of placement is around 40 days.
The retention (completion of the initial assignment) that has been attained within this relationship, is a minimum of 95%.
A Partnership approach with the client is necessary. Having shared goals, ethics and vision make for a successful relationship. Clear communication plans and roadmaps were initiated immediately on award and regular reviews have been set-up to check on progress against the metrics.
Having a Steering Committee set up is also key for the communication flow and to address any higher level issues that arise.
As the relationship grew, metrics were redefined and some changes made for local requirements versus global ones. It is important to continually monitor the issues arising to ensure continual process improvement.
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