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Senior Clinical Trials Manager

CytokineticsSouth San Francisco, California, United StatesOnsite
This job is no longer open

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.

Job Purpose


The Senior Clinical Trials Manager will provide key oversight, guidance, and support for the operation and execution of clinical trials for Cytokinetics clinical program.

Responsibilities


  • Manage various activities associated with multiple clinical studies in accordance with designated project assignments
  • Use thorough knowledge of FDA regulations and ICH guidelines to ensure compliance with both during clinical trial conduct
  • Lead significant Phase II or Phase III program with a focus on clinical operations
  • Design study related documents (or sections therein) including but not limited to: clinical protocols, case report forms, site study manuals, project tools, monitoring plans, tracking tools, informed consent forms
  • Support of departmental functions for preparation and/or attendance at departmental meetings, clinical operations training and developmental activities as required and directed
  • Lead cross-functional study management team meetings, study operations team meetings, and teleconferences with study vendors
  • Manage study-specific CROs and vendors and contract CTMs and CRAs as appropriate
  • Perform independent monitoring of sites as required by needs of project
  • Attend scientific meetings as a representative of Cytokinetics clinical operations team
  • Provide critical insight regarding evaluation and selection of CROs and other outside vendors
  • Coordinate efforts in study start-up, including study feasibility, site selection, preparation and follow-up of site regulatory packages in coordination with other clinical operations staff and other Cytokinetics departments as appropriate
  • Coordinate efforts in all stages of study conduct (enrollment, follow-up, close-out) and oversees clinical operations team and CRO/vendors to ensure the study achieves its goals on time and within budget
  • Collaborate with Finance, Clinical Outsourcing Manager, and line manager on vendor and study site budget tracking and compliance
  • Use well-developed problem-solving skills to address needs of program and provides guidance to other lower level personnel
  • Participate in interviews of Clinical Operations candidates (FTEs and contractors) and provides feedback to hiring manager

Qualifications


  • BA/BS in science-related field with 8+ years’ work experience as a CRA or CRA/CTM combination of relevant related work experience
  • Strong communication skills (verbal and written)
  • Well-developed strong problem-solving skills
  • Demonstrated thorough understanding of FDA regulations and GCP
  • Exceptional interpersonal skills with demonstrated successful team participation
  • Demonstrated skill in managing multiple tasks simultaneously, with attention to detail
  • Ability to work under pressure and deal with time demands; good time management skills
  • Ability to appropriately assess prioritization of assigned activities
  • Ability to proactively identify issues and address with solutions-oriented approach
  • Proficient in use of Microsoft applications such as Word, Excel, Power Point, etc.
  • Ability to travel important as the position could require approximately 20% time spent in business travel

Actual salary at the time of hire may vary and may be above or below the range based on various factors, including, but not limited to, the candidate’s relevant qualifications, skills, and experience, as well as the service line and location where this position may be filled.Salary Pay Range$153,000—$186,000 USDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered.

If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.

Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.  


Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.

Please visit our website at: www.cytokinetics.com


Cytokinetics is an Equal Opportunity Employer



This job is no longer open

Life at Cytokinetics

We are a leading biopharmaceutical company focused on the discovery, development and commercialization of novel small molecule drugs that specifically target the cytoskeleton. The cytoskeleton is a complex biological infrastructure that plays a fundamental role within every human cell. A number of commonly used drugs and a growing body of research validate the role that the cytoskeleton plays in a wide array of human diseases. Our focus on the cytoskeleton enables us to develop novel and potentially safer and more effective classes of drugs directed at treatments for cancer, cardiovascular disease, fungal diseases and other diseases. We have developed a cell biology driven approach and proprietary technologies to evaluate the function of many interacting proteins in the complex environment of the intact human cell. We believe that our approach enhances the speed, efficiency and yield of our drug discovery and development process by accurately and rapidly identifying drug candidates with attractive properties. Our approach has yielded two drug candidates for the treatment of cancer, a drug candidate for the treatment of acute congestive heart failure and more than ten other research programs. Our most advanced drug candidate, SB-715992, is the subject of a broad Phase II clinical trials program designed to evaluate its effectiveness in many different types of cancer. An investigational new drug application, or IND, was filed with the U.S. Food and Drug Administration, or FDA, in 2003 for our second cancer drug candidate, SB-743921, which we expect will enter Phase I clinical development in early 2004. SB-715992 and SB-743921 are being developed through our strategic alliance with GlaxoSmithKline. In addition, we expect to initiate Phase I clinical development for a drug candidate, CK-1213296, for the treatment of acute congestive heart failure in the second half of 2004.
Thrive Here & What We Value1. Passionate about robust scientific thinking grounded in integrity and critical thinking2. Celebrates differences among employees3. Patient-centric approach to all actions and decisions4. Values integrity, ethics, doing the right thing, and being our best selves5. Emphasis on patient-centered care6. Focus on innovation and continuous improvement7. Dedicated to keeping the patient front and center in all actions and decisions8. Values-driven and sustainable approach to drug discovery and development9. Rigorous scientific thinking and critical thinking10. Emphasis on collaboration across different departments and teams
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