Paramount Clinical Research: Clinical Lead, Europe
A global Clinical Research Organisation currently has a number of exciting roles available for Clinical Leads across Europe.
The company are committed to providing solutions that expedite time-to-market and peak-market penetration. With operation in over 50 locations throughout 40+ countries it is a very established and prestigious company to join.

The responsibilities of a Clinical Lead include managing clinical monitoring activities and liaising with project management and the sponsor to ensure that the clinical deliverables are met. The Clinical Lead Role is suitable to either a very experienced Clinical Research Associate II (CRA) or a Senior Clinical Research Associate (CRA) who has demonstrated organizational and leadership skills. Early recognition of areas of potential problems is required and to formulate contingency plans. Evaluate and identifying resourcing needs and provide performance feedback as appropriate, and organize and participating in client, investigator and team meetings. Identifying and facilitating study training needs. Reviewing visit reports, monitoring study timelines and patient recruitment to ensure successful outcome of projects is also required. The Clinical Lead my also be required to monitor site(s) as per client or project request. They will also maintain and assure quality of work generated, and continually monitor budgets to ensure project milestones and budget are achieved. Identifying changes in scope and liaising with Project Manager is also part of the role and compiling monthly reports in a timely manner is essential. Proactively ensuring that all invoicing is completed in a timely manner is part of the Clinical Lead role and effectively communicating with internal and external customers as well as third party vendors.

To be considered and work as a Clinical Lead you must have the following skills and experience;
- A degree in a life science, medical, nursing or related qualification
- Ideally 4 years’ experience in clinical research including around 1-2 years of proven experience in coordinating clinical trials is essential
- Previous experience in clinical research including proven experience in monitoring clinical trials
- Possess strong negotiation, diplomacy, team leadership skills and excellent organizational ability
- Ability to motivate both individuals and a team
- Excellent English, written and oral communication skills in addition to local language
- The ability to complete tasks in an accurate, timely manner and effectively manage multiple tasks
- The ability to identify and address issues proactively in a timely manner
- A financial understanding and ability to manage a budget
- The ability to take initiative, work independently and delegate
- Accountability for all assigned tasks

With the above experience this is a very good opportunity for an experienced Clinical Research Associate II (CRA) or Senior Clinical Research Associate (CRA) to join a great company and develop their experience. You will have fantastic support for career development.

For more information call Gareth on +44(0)121 616 5135 or apply now for more details.

Keywords - Clinical Research Associate (CRA), clinical, clinical research, clinical research associate, senior CRA, senior clinical research, clinical trials, clinical study, clinical studies, clinical associate, clinical monitor, clinical project, project manager, CRA, CPM

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