drjobs Director Drug Safety Operations

Director Drug Safety Operations

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

South San Francisco, CA - USA

Monthly Salary drjobs

$ 251800 - 278300

Vacancy

1 Vacancy

Job Description

Cytokinetics is a latestage specialty cardiovascular biopharmaceutical company focused on discovering developing and commercializing firstinclass muscle activators and nextinclass 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.

This position will provide leadership and direction to the Drug Safety operations for adverse event case management support of study teams and projects oversight of maintenance of drug safety database and collaboration to support risk management and pharmacovigilance for all Cytokinetics clinical trials.

Responsibilities

Manage SAE/SUSAR reporting activities for all investigational

Manage preparation and processing of internal and external SAE reports

Review incoming adverse events to determine action required

Oversee maintenance of a hosted electronic database for tracking storing and reporting serious adverse events from Cytokinetics clinical trials.

Ensure corporate compliance with domestic and international adverse event reporting requirements for all products in worldwide development programs

Collaborate with partners on the exchange of safety data safety monitoring and the safety profile of investigational as defined in Pharmacovigilance Agreements

Lead preparation of safetyrelated plans with partners and CROs

Provide guidance and support to project teams for safetyrelated areas including protocol development and study conduct

Contribute to preparation of relevant sections of clinical study reports annual reports expedited safety reports and other regulatory filing documents

Coordinates pharmacovigilance Quality Auditing preparation

Coordinates root cause analysis and implementation of corrective action and preventing action (CAPA) after internal audits and inspections

Assist with preparation and updates to Investigator Brochures DSURs Protocols ICFs etc.

Train staff and external CROs on drug safety principles and procedures

Manage and mentor staff and assign responsibilities as appropriate to meet timelines and quality metrics

Respond to safetyrelated queries from regulatory authorities or Ethics Committees if needed

Collaborate to ensure alignment among case handling aggregate reporting and signal detection activities


Qualifications

Advanced degree in life sciences nursing pharmacy or medicine

10 years pharmaceutical industry drug safety experience

Knowledge of and experience with international regulatory adverse event reporting requirements

EudraVigilance electronic reporting of ICSRs experience

Handson experience with adverse event case processing

Proven experience and effectiveness at training and mentoring drug safety staff Excellent knowledge of MedDRA coding and WHODrug coding

Ability to work independently establish functional priorities and execute on goals

Excellent interpersonal communication skills and ability to work effectively as part of teams

Experience in neurology and/or cardiovascular drug development desirable

Pay Range:

In the U.S. the hiring pay range for fully qualified candidates is $251800.00 $278300.00 USD Annual USD per year. The base pay actually offered will take into account internal equity and also may vary depending on the candidates geographic region jobrelated knowledge skills and experience among other factors.

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 ourGeneral Data Protection Regulation (GDPR) policyPRIOR 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.

Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers

Recently there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain and will only be made after completing a formal interview process.

Here are some ways to check for authenticity:

Please visit our website at:

Cytokinetics is an Equal Opportunity Employer


Required Experience:

Director

Employment Type

Full-Time

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.