- 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
- 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
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Senior Clinical Trials Manager - South San Francisco, United States - Cytokinetics
Description
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
Salary Pay Range
$153,000-$186,000 USD
Our 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:
Cytokinetics is an Equal Opportunity Employer