drjobs Senior Drug Safety Case Manager

Senior Drug Safety Case Manager

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

Not Disclosed

drjobs

Salary Not Disclosed

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.

The Senior Drug Safety Case Manager will independently support the Drug Safety Department. The candidate will work in a role of leadership in development implementation and maintenance of a quality system for all Drug Safety activities encompassing processes procedures compliance and metrics.

Responsibilities

  • Assist in overseeing the CRO processing SAE reports on Cytokinetics products in accordance with all applicable regulations guidelines and SOPs with little or no supervision. This includes detailed review of source documentation assessing cases for reportability generation of analysis of similar events quality check and overseeing preparation of applicable aggregate safety reports.
  • Evaluate project or case workflow and offer solutions for process improvement
  • Maintain regulatory and department compliance by ensuring timely completion of reports and assisting in submissions of reportable cases to regulatory agencies (if needed) study investigators and licensing partners
  • Represent the Drug Safety Department in crossfunctional team meetings as needed
  • Support coding review of medical history adverse events and concomitant medications
  • Conduct periodic reconciliation of SAEs between the drug safety and clinical trial databases for ongoing clinical studies.
  • Draft and update departmental SOPs and other work practices as assigned and maintain consistency with regulatory guidelines and good pharmacovigilance practices
  • Participate in training internal and external audiences on drug safetyrelated topics as assigned.
  • Guide departmental policies and procedures by maintaining a high level of understanding of federal and international regulations
  • Draw upon the knowledge of Drug Safety regulations & practices diseasespecific clinical knowledge and understanding of corporate objectives to solve complex problems in creative and effective ways as well as to anticipate routine problems and mitigate them without supervisory intervention

Qualifications

  • BS degree in a life science discipline (e.g. pharmacy or nursing) with 5 years of relevant experience
  • Broad knowledge of domestic and international drug safety regulations industry practices and standards
  • Must have a strong attention to detail teamwork and initiative
  • Must have excellent written and oral communication skills resourcefulness and personal organization skills
  • Excellent working knowledge of MedDRA and WHODRUG coding dictionaries.
  • PC literacy required; MSOffice skills (Outlook Word Excel PowerPoint)

Pay Range:

In the U.S. the hiring pay range for fully qualified candidates is $161500 $178500 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:

Manager

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.