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Excellent Job Opportunity for the position of Sr. Clinical Trial Manager (6419334)
Ref No.: 17-44068
Location: San Francisco, California
Position Type:Contract
Start Date: 03/06/2017
Job Title: Sr. Clinical Trial Manager (JOB ID- 6419334)
Location:
San Francisco, CA
Duration: 03 Months
Client: A Big Pharmaceutical Company


Job Description:
The Senior Clinical Trial Manager will independently manage all components of a clinical trial. The assigned clinical trial(s) may be highly complex.
The Senior Clinical Trial Manager is accountable for ensuring clinical trial activities and deliverables are completed on-time, within budget, and in a highly dynamic and complex environment in accordance with appropriate quality standards including GCP/ICH requirements and Client SOPs.
Oversee and manage all aspects of a clinical trial in accordance with Client SOPs, ICH/GCP regulations and study-specific manuals and procedures.
Participates in Study Management Team(s), including cross-functional team(s), CRO(s) and third-party vendors as applicable. Develop and manage effective relationships with key study stakeholders.
Responsible for key study quality metrics (i.e., eligibility, primary endpoint data, etc.). Participates in the identification, evaluation and hiring of appropriate CROs and other third party study vendors in accordance with Client SOPs.
Works with CROs and other third party vendors, including setting expectations, training, managing timelines and deliverables, and issue management.
Manage the clinical study budget, ensuring the project remains within scope and that out of scope activities are identified and handled appropriately.
In collaboration with the Study Management Team, identify risks to study and develop risk mitigation plans, including communication with senior management when necessary.
Contributes to preparation of clinical protocols, informed consent forms, study manuals, case report forms, and other clinical research related documents.
Ensure clinical data are reviewed in accordance with study data review plans and that a final, clean dataset is provided upon database lock.
Project and coordinate study supply and packaging requirements.
Provide weekly enrollment and program updates to senior management.
Identify and share best practices and process improvements with colleagues to ensure optimal efficiency and consistency in Clinical Operations.

Skills:
Must have demonstrated problem solving abilities and strong organizational skills. Excellent written and verbal communication skills are required. Strong computer skills (MS Office) are required. Excellent working knowledge of FDA & ICH GCP regulations and guidelines is required.
Must be a demonstrated self-starter and team player with strong interpersonal skills.
Must possess excellent cross-functional clinical project management skills.
Demonstrated ability to develop and implement SOPs and Study Plans.
Strong experience working as a Clinical Research Associate is preferred and thorough knowledge of clinical monitoring practices is required.
Fluent English is required.

Education:
A Bachelor's degree or equivalent is required (life science degree is preferred). Typically an average of 8-10 years in the pharmaceutical industry is required, including but not limited to 4 years overseeing trial management.

Interested candidates can share their most updated resume at wajid.khan@artechinfo.com or they can reach out to me on #973-967-3412 Ext:3412