- Integrated Resources, Inc (Cambridge, MA)
- …Cambridge, MA Duration: 8+ Months Job Description: Duties: . Reporting to the Associate Director , Drug Safety and Pharmacovigilance Compliance and ... Operations, you will play a pivotal role in drug safety activities, supporting records management and compliance across the clinical development and marketing programs. You will be a key contributor to the day-to-day operational activities of the department,… more
- Boehringer Ingelheim (Athens, GA)
- **Description** The AD Global PV Data Analysis supports the Global Pharmacovigilance (PV) team to ensure compliance with all regulations and laws worldwide on ... Pharmacovigilance (including but not limited to FDA 21 CFR,...data internally as to the Health authorities. + Providing Pharmacovigilance Information (RPI) as requested to other departments within… more
- AbbVie (North Chicago, IL)
- …Instagram, YouTube and LinkedIn. Job Description Purpose: Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading Product ... signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Responsibilities: + Understanding… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... accredited institution and more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or DO degree or international… more
- Lilly (Indianapolis, IN)
- …develop creative solutions to support communities through philanthropy and volunteerism. Associate Director / Director , External Collaborations will lead ... Lilly marketed products and compounds in development. **Responsibilities:** Drive Pharmacovigilance /Regulatory partnership strategy + Define strategy for business partnerships… more
- Merck (West Point, PA)
- …will be responsible for managing the development and implementation of pharmacovigilance strategies, processes, and systems for a pharmaceutical company, ensuring ... PV strategies: Work with cross-functional teams to develop and implement pharmacovigilance strategies that meet regulatory requirements and ensure patient safety,… more
- Bristol Myers Squibb (Princeton, NJ)
- …medicines: The Worldwide Patient Safety group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety ... documents for new and expanded indications (Filing Activities). Ensures pharmacovigilance regulatory compliance. Mentors less experienced scientists and teams in… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... the global Inflammation Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or… more
- Lilly (Indianapolis, IN)
- …and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage clinical and scientific expertise ... sources + Consult and coordinate with the Device Surveillance Senior/Executive Director and Device Safety Physician to facilitate appropriate signal management of… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Associate Director , External Research, Scientific Affairs provides strong subject matter expertise, operational oversight and process ... process. + ER Trial Protocol + Leads and works cross functionally with Global Pharmacovigilance , CDMA TA Medical, and RA to review the trial protocol and ensure that… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** **Sr. Associate Director Requirements:** + US MD or DO degree or ... the global CREA Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...years of applicable experience, required. + Leadership experience required. ** Director Requirements:** + US MD or DO degree or… more
- Bristol Myers Squibb (Minneapolis, MN)
- …and spirit of independence and love of challenge. **Job Description** The Region Director (RD) is a remote leadership position that is primarily responsible for ... satisfaction and productivity. This position reports into a national Field Medical Director role. The RD position is underpinned with the expectation of leadership… more
- AbbVie (North Chicago, IL)
- …Description In collaboration with a therapeutic area Medical Director or Scientific Director , the Associate Director or Clinical Scientist II, will lead ... the design, conduct, analysis, and reporting of clinical trials. The Associate Director , Clinical Science will apply scientific training and clinical research… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Medicine. You will focus on Medical Affairs, Patient Safety and Pharmacovigilance (PSPV), Regulatory Affairs, and Epidemiology. In more detail, this includes ... pharmaceutical industry in a relevant medicine function (Medical Affairs, Pharmacovigilance , Regulatory Affairs, Epidemiology, Clinical Operations and Development). +… more
- Bristol Myers Squibb (Trenton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . Position: Regional Associate Director Location: Central Region - MGG Team The Field ... data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing… more
- Lilly (Indianapolis, IN)
- …may impact a positive benefit-risk balance for a given product. The Associate Director Pharmacoepidemiology Study Operations (AD Ops)is responsible for providing ... as well as vendor selection decisions. + Work closely with PE Sr Director and/or delegates to identify operational gaps & drive solutions department-wide. + Build… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , Medical Coding, Analytics & Process is responsible for ... conventions and related trainings. + Firm knowledge of regulatory environment in Pharmacovigilance and GCP. + Experience with clinical trial databases and/or PV… more
- ThermoFisher Scientific (Wilmington, NC)
- …to 1-2 years) in the industry. + Direct experience in safety/ Pharmacovigilance (comparable to 2 years). + Candidates with industry experience(CRO/Pharma) maybe ... considered for Medical Director /Senior Medical Director level. _In some cases an equivalency, consisting of a combination of appropriate education, training… more
- Boehringer Ingelheim (Ridgefield, CT)
- …evidence team (Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance , Regulatory, Medical Affairs, Market Access, Epidemiology, RWE ... requirements and global regulatory and ethical standards. **Requirements** **Requirements for Director Level:** + MD and retinal specialist from an accredited… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS) ... for assigned products. This position drives/leads the maintenance of global labeling and associated documents (including cartons and external packaging in the US) for assigned Daiichi Sankyo products. This position ensures that draft labeling complies with all… more
