Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
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Regeneron Pharmaceuticals Temp - Senior Manager Clinical Study Lead (Oncology) in Uxbridge, United Kingdom

As a Temp Senior Clinical Study Lead (SCSL), you will lead the cross-functional study team responsible for the global execution of large, complex clinical trials from study design through study close out. These responsibilities apply to both internally sourced studies and studies outsourced to CROs, so we need a Temp SCSL who has experience managing Third-Party Vendors. We need someone who can also contribute to and drive process improvement initiatives that support our rapidly growing organization. This is an exciting time to join our organization and have a direct impact on bringing life-saving treatments to the market.

As a SCSL, a typical day might include the following:

  • Providing operational input into protocol development

  • Leading all aspects of and contributing to the development of study specific documentation e.g. case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.

  • Supervising set-up and maintenance of study systems such as Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.

  • Ensuring compliance with the clinical trial registry requirements

  • Providing input into baseline budget and timeline development and managing the study against planned budget, timeline and results

  • Leading risk assessment and identifies risk mitigation strategies at the study level

  • Managing feasibility assessment to select relevant regions and countries for the study

  • Conducting site evaluation and selection

  • Leading investigator meeting preparation and execution

  • Monitoring progress for site activation and monitoring visits and acts on any deviations from plan

  • Managing development and implementation of patient recruitment and patient retention strategies

  • Monitoring data entry and query resolution and taking action on any divergence from agreed metrics

  • Overseeing and providing input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation

  • Raising issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other partners and developing and implementing appropriate actions to address issues

  • Ensuring data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites

  • Ensuring clinical project audit and inspection readiness through the study lifecycle and contributing to CAPAs as required

  • Supervising study close-out activities and contributing to clinical study report writing and review

  • Directly supervising Clinical Trial Management staff, including assigning work, performance management, recruitment, mentoring and professional development

This role might be for you if:

  • Have direct management experience with demonstrated results building and developing outstanding teams along with the capacity to understand and implement the strategic direction and guidance for respective clinical studies

  • Can take a proactive and self-disciplined approach to managing projects with a developed ability to meet deadlines and prioritize

  • Have a history of effectively leading and negotiating with vendors

  • Have a data-driven approach to planning, executing and problem solving

  • Operate with a high degree of cross-functional agility using exceptional influencing and interpersonal skills

  • Have the innate ability to rally disparate groups to accomplish lofty shared goals

To be considered for this opportunity you must possess a Bachelors’ degree with a minimum of 8 years of relevant industry experience. Advanced degrees may be considered in lieu of industry experience. Direct experience managing global clinical trial operations is a must, including experience developing protocols and key study documents. You will also need technical proficiency trial management software and MS applications.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.

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