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Sr Mgr, Clinical Safety

Irvine, CA 92614

Posted: 07/31/2024 Employment Type: Contract Job Category: Pharmacovigilance Job Number: 609113 Is job remote?: No Country: United States

Job Description

Target PR Range: 61-71/hr
*Depending on experience
 
Key Responsibilities:
  • Conduct Sponsor assessment of adverse events and device deficiencies reported through clinical studies (e.g. assessment of seriousness, relationship to device and procedure, and UADE (Unanticipated Adverse Device Effect) determinations). Determine what additional information is required for comprehensive assessment and adjudication, when required. Interact with site coordinators and trial managers for the purposes of safety data collection and data reconciliation.
  • Report adverse events and complaints according to regulatory requirements, trial safety processes and procedures. Respond to related questions from regulatory authorities.
  • Draft/Design charters and provide oversight of internal and external CEC and DSMB/DMC process. Perform quality assurance of adjudication results and output
  • Design CEC and DSMB/DMC charters, provide safety/regulatory and medical expertise to Quality Compliance/Complaint Handling on medical aspects of reported complaint information
  • Prepare or review complex event narratives for internal review (e.g. R&D, quality, RA) or external review (Clinical Endpoints Committee), as well as for regulatory submissions. Review and analyze aggregate safety reports to identify early safety signals and escalate to leadership with recommended next steps.
  • Create clinical risk/benefit analysis documents to meet internal and regulatory requirements. Provide input on clinical trial design and develop safety sections of study protocols, regulatory submissions, and clinical/regulatory reports
  • Represent safety in cross-functional and core team meetings. Represent safety in internal and external audits
  • Develop training materials and train and site personnel and safety committees on compliant safety reporting and appropriate support documentation.
  • Other incidental duties

Education and Experience: Other: in Physician Assistant (PA) with a Master's degree in Physician Assistant Studies (MPAS), Health Science (MHS), or Medical Science (MMSc) or Nurse Practitioner (NP) with a Master's of Science in Nursing (MSN) or advanced practice registered nurse (APRN) or equivalent, 8 years experience of combined medical/clinical and relevant industry experience Required or

Other: in M.D, DO or equivalent, 5 year's experience of relevant medical/clinical and relevant industry experience Required

Experience in internal medicine/cardiology/cardiac surgery Preferred

Experience with Medical Device Preferred

Additional Skills:
  • Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with KOLs and clinical personnel
  • Ability to translate complex and technical information to project team management and key leadership
  • Recognized as an expert in own area within the organization while applying broad-based technical expertise, and has knowledge of other related disciplines
  • Expert knowledge of cardiovascular anatomy, pathology and physiology
  • Expert understanding of principles of regulatory requirements and adverse events reporting
  • In-depth understanding of corporate/global procedures, standard operating procedures, and writing practices
  • Leadership skills and ability to influence change
  • Knowledge of and adherence to Environmental Health and Safety and Quality guidelines
  • Strict attention to detail
  • Ability to interact professionally with all organizational levels
  • Ability to manage competing priorities in a fast paced environment
  • Represents organization as key medical contact on projects including physicians and clinicians; R&D, quality, RA, etc.
  • Must be able to work in and help lead in a team environment
  • Medical liaison with external physicians and clinicians
  • Provides expert medical input to help provide solutions to difficult technical issues and help drive organizational projects
  • Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

The staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.

Planet Pharma is an equal opportunity employer. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.

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Although this hasn't been an issue at Planet Pharma, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.