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Clinical Operations Manager (Oncology Experience Required)
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$105k-137k (estimate)
Full Time 6 Days Ago
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Scorpion Therapeutics is Hiring a Clinical Operations Manager (Oncology Experience Required) Near Boston, MA

Scorpion is a pioneering clinical-stage oncology company redefining the frontier of precision medicine to deliver optimized and transformational therapies for larger populations of patients with cancer. Scorpion has built a proprietary and fully integrated platform of the most advanced technologies across cancer biology, medicinal chemistry, and data sciences, with the goal of consistently and rapidly creating exquisitely selective small molecule compounds against an unprecedented spectrum of targets. Scorpion aims to leverage its platform to advance a broad pipeline of wholly owned, optimized compounds across three target categories: best-in-class molecules targeting validated oncogene targets; first-in-class molecules for previously undruggable targets; and first-in-class molecules for novel cancer targets.
Job Summary :
In this important role within Clinical Operations, the manager is responsible for collaborating with clinical and regulatory functions to execute on clinical strategies to deliver successful operational outcomes across one or multiple clinical trials. The manager will work with the Clinical Study Lead to ensure on time delivery of key tasks within a clinical study. In addition to exceptional project delivery, we seek strong analytical skills, attention to detail, and leadership qualities that will influence our internal team and motivate our CRO partners. The ideal candidate values bringing important medicines to patients in need, and shares our team's determined, positive attitude.
Role Responsibilities/Accountabilities :
  • Devise and implement efficient, effective clinical trial execution strategies; inform planning and monitor execution of clinical studies, including management of study budgets / timelines and external vendor(s) management.
  • Provide internal updates on trial progress to leadership with respect to project plans, timeline, budgets, quality standards, and regulatory compliance.
  • In collaboration with the Clinical Study Lead, Program level clinical operations leadership, and CRO (if applicable), ensure procedures and support are available to facilitate delivery of high-quality clinical data.
  • Ensure compliance of clinical trials with federal and applicable regulatory agency requirements.
  • Facilitate expert review and manage the generation, approval, and control of trial documentation, including but not limited to invoices, protocol, and informed consent documentation.
  • Successfully partner with and oversee the CRO and their conduct of the clinical study (if applicable).
  • Facilitate data lock and transfer of data for analysis. Coordinate data analysis and reporting in an efficient and timely manner. Complete trial reporting compliant to regulatory requirements.
  • Ensure all project level documentation is filed in accordance with SOPs/regulatory requirements including archiving and maintenance.
Background/Experience and Education:
  • BS/MS in science or a health-related field is preferred.
  • Preferably 4 or more years related work experience, with at least 2 years in a study management role. Biopharmaceutical (Sponsor) organization experience is a preferred.
  • Demonstrated effectiveness in resolving study management issues.
  • Experience managing a broad project team in a matrix setting is required; direct line management is not required.
  • In-depth knowledge of the CRO management strategies is required.
  • Strong communication, project management, and data analysis skills;
  • Must have thorough understanding of GCP and ICH regulations, clinical trial monitoring, and regulatory compliance.
  • Prior NDA/BLA submission experience is desirable.
  • Prior experience in Oncology drug development and Phase 1 trial execution is desirable.
  • Up to 30% travel may be required to research sites, investigator meetings or vendor meetings. International travel may be required.
Scorpion Therapeutics Inc. is an Equal Opportunity Employer who strives to create and maintain a diverse working environment. We do not discriminate for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Beginning October 13, 2021, Scorpion Therapeutics requires all new hires to be fully vaccinated against COVID-19. If you are unable to receive the vaccine due to a disability or serious medical condition, or because of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.

Job Summary

JOB TYPE

Full Time

SALARY

$105k-137k (estimate)

POST DATE

06/26/2024

EXPIRATION DATE

07/13/2024

WEBSITE

scorpiontx.com

HEADQUARTERS

BOSTON, MA

SIZE

25 - 50

FOUNDED

2020

TYPE

Private

CEO

CLAUDIO NESSI

REVENUE

<$5M

INDUSTRY

Business Services

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About Scorpion Therapeutics

Scorpion Therapeutics is a pharmaceutical firm that researches and commercializes therapeutics for the treatment of oncology.

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The following is the career advancement route for Clinical Operations Manager (Oncology Experience Required) positions, which can be used as a reference in future career path planning. As a Clinical Operations Manager (Oncology Experience Required), it can be promoted into senior positions as a House Supervisor that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Operations Manager (Oncology Experience Required). You can explore the career advancement for a Clinical Operations Manager (Oncology Experience Required) below and select your interested title to get hiring information.

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