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Senior Clinical Lead
- Permanent
- Program Manager / Director
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting a Senior Clinical Lead for a CRO located in New York, NY. Successful candidate will provide leadership of the clinical team, in support of the project leader to achieve the delivery of the project's overall objectives.
Job Responsibilities:
- Accountable for ensuring the "right subjects" and "right data" to meet our contractual requirements.
- Participate in bid defense preparations. Attend bid defense presentations and lead the clinical delivery strategy for medium size and multiple country/region studies, in partnership with business development and senior project leader as needed.
- Monitor clinical progress against contract and prepare/present project information proactively to all stakeholders internally and externally as required.
- Deliver the project/program according to the quality management plan. Guide CRAs and advise on critical specific study issues.
- Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
- Manage risks (positive and negative) which could impact on the clinical delivery of the project and determine contingencies. Partner with functional leaders in problem solving and resolution efforts.
- Serve as clinical project contact with customer where applicable and agreed with the project leader.
- Drive for high performance and efficiency of the clinical team to support financial success of the project.
- Support the project leader in ensuring the financial success of the project.
- Identify changes in scope and support project leader in completion of the change control process.
- Identify and communicate lessons learned and implement best practices to promote continuous improvement.
- Adopt corporate initiatives and changes and serve as a change advocate when necessary.
- All responsibilities are essential job functions unless noted as nonessential (N).
Skills and Responsibilities:
- Bachelor's degree in a health care or other scientific discipline with 7 years clinical research/monitoring experience; or equivalent combination of education, training and experience.
- In depth knowledge of, and skill in applying applicable clinical research regulatory requirements.
- Broad protocol knowledge; therapeutic knowledge
- Strong understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates
- Ability to understand customer needs and appropriately influence decision making
- Good understanding of other company functions and their inter-relationship to achieve project delivery
- Knowledge of Project management practices and terminology
- Ability to develop and deliver training materials to achieve clinical team understanding of project and enable effective delivery thereof
- Good understanding of project financials
- Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving
- Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues
- Extensive use of telephone and face-to-face communication requiring accurate perception of speech
- Extensive use of keyboard requiring repetitive motion of fingers
- Regular sitting for extended periods of time
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Susan Chapman at (+1) 646-542-0158 or upload your resume on our website - www.proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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#Clinical
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