Merck

To make a difference in the lives of people globally through our innovative medicines, vaccines, and animal health products. We are committed to being the premier, research-intensive biopharmaceutical company and are dedicated to providing leading innovations and solutions for today and the future.

Merck Remote * (Rahway, NJ 07065, USA)
Apr 06, 2021
Job Description Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. Primary Responsibilities Assumes the responsibilities for Clinical database development deliverables including database set-up and edit check programming to support multiple clinical programs. Coordinates and participates in the following activities: Accountable for the clinical database design activities for the startup of a protocol which include design and implementation of clinical database for electronically captured data. Participates in the review of Electronic Case Report Forms ( eCRFs) and edit checks, database development, programming of edit checks. Review the technical feasibility of study team...
Merck Remote * (West Point, PA, USA)
Apr 06, 2021
Job Description Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Direct a team of professionals that are skilled and capable of providing expertise in the design and application of statistical and mathematical methods to the our company. The incumbent will, individually and through assignment of staff, provide statistical expertise on experimental design, and the evaluation and interpretation of data. The incumbent will also direct staff in the evaluation of data for submission to regulatory agencies and pharmacopoeia. The person will serve on various company task forces and outside industry groups to influence regulatory policies. Primary...
Merck Remote * (1130 N Bethlehem Pike, Spring House, PA 19477, USA)
Apr 06, 2021
Job DescriptionUnder the general direction of the Clinical Safety and Risk Management (CSRM) Group Lead, the CSRM Physician is an expert in assigned Therapeutic Area and is responsible for the overall clinical risk management and safety surveillance of assigned investigational and marketed products within Therapeutic Area. This includes all aspects of safety monitoring including assessing safety information and ensuring completeness of safety information in worldwide package circulars. The incumbent is also responsible for the development of post-market risk management plans and pharmacovigilance strategies/specifications.The incumbent is a member of the Product Development Teams and chairs the Risk Management and Safety sub-team for assigned products. Partners with appropriate company departments and therapeutic area head to ensure efforts are aligned to meet our global risk management strategies for assigned products. Works with CSRM Group Lead to plan direction for risk...
Merck Remote * (Rahway, NJ 07065, USA)
Apr 06, 2021
Job Description Our Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. This role is primarily accountable for the end to end performance and project management for assigned protocols in a country in compliance with International Conference on Harmonisation Good Clinical Practice (ICH/GCP) and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. For certain studies, the Clinical Research Manager (CRM) could be responsible for several countries in a cluster. Responsibilities include, but are not limited to: Main Point of Contact (POC) for assigned protocols and links between Country Operations and clinical trial team (CTT). Responsible for project...
Merck Remote * (Rahway, NJ 07065, USA)
Apr 06, 2021
Job DescriptionPosition PurposeClinical Safety Physician Under the general direction of the Clinical Safety and Risk Management Group Lead, the CSRM Physician is an is responsible for the overall clinical risk management and safety surveillance of assigned investigational and marketed products. This includes all aspects of safety monitoring including assessing safety information and ensuring completeness of safety information in worldwide package circulars. The incumbent is also responsible for the development of post-market risk management plans and pharmacovigilance strategies/specifications.Primary ResponsibilitiesThe incumbent is a member of the Product Development Teams and chairs the Risk Management and Safety sub team for assigned products. Partners with appropriate company departments and therapeutic area heads to ensure efforts are aligned to meet our global risk management strategies for assigned products. Works with CSRM Group Lead to plan direction for risk management...
Merck Remote * (Boston, MA, USA)
Apr 06, 2021
Job Description Our Oncology team is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of forward-thinking individuals achieve this through an unwavering commitment to support accessibility to medicine, providing new therapeutic solutions, and collaborating with governments and payers to ensure that people who need medicines have access to them. Our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. IMPACT OUR TEAM! Our Medical Writing department strives to be the premier regulatory documentation organization in the biopharmaceutical industry. Our Medical Writers are integral to helping bring medical breakthroughs to the world. We rely on expert skills and inventiveness to realize this life-saving goal. The Managing Medical Writer is responsible for development and management of medical writing...
Merck Remote * (West Point, PA, USA)
Apr 06, 2021
Job Description Our team seeks to unleash the power of the statistics and data science in late stage product development and manufacturing. We aspire to be drivers of innovation and digitalization, as well as thought leaders in Chemistry, Manufacturing and Controls (CMC) data analytics to save and improve lives. Position Description: You will be an advocate for Chemistry, Manufacturing and Controls (CMC) statistics and data science and serve as a consultant to engineers, scientists and principals in the manufacturing division. You will be a key member of cross functional teams and will provide statistical and data science sponsorship for designing experiments, modeling structured and unstructured data, and constructing data visualizations. You will provide technical management in design of experiments (DOE), analysis of data, statistical process control (SPC), simulation, design of sampling plans, and problem solving. You will also evaluate data for submissions and replies...
Merck Remote * (West Point, PA, USA)
Apr 06, 2021
Full-Time
Job Description In partnership with the Quality Assurance Lead (QAL), the Quality Assurance Specialist (QAS) will support the implementation and management of the Quality assurance strategy across multiple studies, and/or countries. The QAS will utilize audit and inspection intelligence and risk mitigation plans to assure adherence to Good Clinical Practice (GCP) in the conduct of clinical trials, the quality and integrity of generated data, and the rights and welfare of subjects/patients. The QAS position is responsible for the execution of the global Quality Assurance (QA) audit activities on assigned studies/products/vendors/Country Offices (CO). This role is accountable for Good Clinical Practice (GCP) and/or Pharmacovigilance (PV) oversight, and for assuring the compliance of studies with our Company's Standard Operating Procedures (SOPs), policies, and all applicable worldwide regulations and guidelines (e.g., United States FDA, European Union Directives, ICH, and National...
Merck Remote * (West Point, PA, USA)
Apr 06, 2021
Job Description The ideal candidate will serve as a consultant and advocate of Chemical Manufacturing Controls (CMC) Statistics to technical specialists and managers in our Company's pharmaceutical, biologic and vaccine manufacturing. You will be a key member of teams developing, validating, and transferring bioassays and promoting stability evaluations. The candidate will provide technical direction in tasks that include the design of experiments (DOE), dissection of data, statistical process control (SPC), simulation, design of sampling plans, and problem-solving. You will also evaluate data for submissions and replies to regulatory agencies and pharmacopeia. Qualifications Minimum Education: M.S. in Statistics (or equivalent) with 15 years of relevant applied work experience or a minimum of 5 years with PhD Skills: Coursework should include industrial statistics (DOE, SPC, regression, general linear models, and multivariate methods). Promoting systematic method...
Merck Remote * (Rahway, NJ 07065, USA)
Apr 06, 2021
Job Description Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.This role serves as a key internal and external representative for US. This role will also be assigned as the primary point of contact for 10-25 high-performing sites as collaborative partners in the successful execution of company trials across all therapeutic areas, building professional, productive relationships, placing our company as a partner of choice among these key sites. Strategically supports initiatives with a solution-oriented focus to overcome challenges with sites and innovation with Global Clinical Trial Operations (GCTO-US). Responsibilities include, but are not limited to: Establishes and fosters effective relationships with internal and external stakeholders,...
Merck Remote * (Carolina, NC, USA)
Apr 04, 2021
Full-Time
Job Description Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines, and new indications for existing products. We ensure we conduct high-quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. We care deeply about helping the world be well. We strive to improve health for others in the future by developing new drugs and vaccines that treat and prevent disease. Clinical trials are an essential part of this process. The Senior Clinical Research Associate role is integral to helping the world meet new breakthroughs that affect generations to come, and we're counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Core tasks, including but not limited to, the following: Acts as primary site contact and site manager throughout all phases of a clinical...
Merck Remote * (De Soto, KS, USA)
Apr 04, 2021
Job Description Our Animal Health Marketing team takes a customer centric perspective using customer feedback and market intelligence data. Using this data, we design, develop and deploy products, platforms, brands and marketing initiatives that ensure we can improve the health and well-being of animals everywhere. Essential Accountabilities: A background in e-commerce/retail/channel account management, product management, project management, financial analysis, forecast and supply Excellent customer service skills that support customers and our company's Animal Health's product portfolio Build cross functional relationships across multiple business divisions, including legal, finance, Pharmacovigilance, brand, credit, operations and supply to support business and channel development Strong communication skills and ability to connect with defined accounts Remain knowledgeable about relevant trends and innovations in e-commerce/retail Creating promotional...
Merck Remote * (Lansdale, PA, USA)
Apr 04, 2021
Job DescriptionUnder the general direction of the Clinical Safety and Risk Management (CSRM) Group Lead, the CSRM Physician is an expert in assigned Therapeutic Area and is responsible for the overall clinical risk management and safety surveillance of assigned investigational and marketed products within Therapeutic Area. This includes all aspects of safety monitoring including assessing safety information and ensuring completeness of safety information in worldwide package circulars. The incumbent is also responsible for the development of post-market risk management plans and pharmacovigilance strategies/specifications. The incumbent is a member of the Product Development Teams and chairs the Risk Management and Safety sub-team for assigned products. Partners with appropriate company departments and therapeutic area head to ensure efforts are aligned to meet our global risk management strategies for assigned products. Works with CSRM Group Lead to plan direction for risk...
Merck Remote * (Carolina, NC, USA)
Apr 03, 2021
Full-Time
Job Description Our Oncology team is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of forward-thinking individuals achieve this through an unwavering commitment to support accessibility to medicine, providing new therapeutic solutions, and collaborating with governments and payers to ensure that people who need medicines have access to them. Our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people with cancer across the globe. Impact our team as a Medical Writer! Our Medical Writing Department strives to be the premier regulatory documentation organization in the bio-pharmaceutical industry. Our Medical Writers are integral to helping bring medical breakthroughs to the world. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, and...
Merck Remote * (Chicago, IL, USA)
Apr 03, 2021
Job Description Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines, and new indications for existing products. We ensure we conduct high-quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. We care deeply about helping the world be well. We strive to improve health for others in the future by developing new drugs and vaccines that treat and prevent disease. Clinical trials are an essential part of this process. The Senior Clinical Research Associate role is integral to helping the world meet new breakthroughs that affect generations to come, and we're counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Core tasks, including but not limited to, the following: Acts as primary site contact and site manager throughout all phases of a clinical...