• Merck & Co. (Rahway, NJ)
    …the clinical /scientific execution of clinical protocol(s).Serves as the lead clinical scientist on the clinical trial team.Collaborates with the ... Job DescriptionPosition Description: Associate Director, Clinical Scientist This position...prioritization skillsAdvanced analytical skills with the ability to interpret clinical trial data andsynthesize conclusionsInteract with key… more
    HireLifeScience (11/05/24)
    - Save Job - Related Jobs - Block Source
  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... leader (CSL)Study Planning and Execution: Provides input on major milestones of trial , clinical trial plan and contingency planning; Analyzes and updates… more
    HireLifeScience (11/12/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (Rahway, NJ)
    …team members including clinical directors and study managers to lead/support clinical trial scientific activities in the Atherosclerosis & Metabolism TA.Job ... /scientific execution of clinical protocol(s). Serves as the lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on … more
    HireLifeScience (11/13/24)
    - Save Job - Related Jobs - Block Source
  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
    HireLifeScience (11/14/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (Rahway, NJ)
    clinical development strategies for investigational drugs and planning clinical trials (design, operational plans, settings) based on these ... development strategiesMonitoring and managing the conduct of ongoing or new clinical trials for investigational drugsAnalyzing and summarizing the clinical more
    HireLifeScience (11/14/24)
    - Save Job - Related Jobs - Block Source
  • Genmab (Plainsboro, NJ)
    …synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners ... trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
    HireLifeScience (10/18/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (Rahway, NJ)
    …Mass Spectrometry based assays that are deployed in support of clinical trials . The candidate for this Associate Principal Scientist position should have ... and late-stage clinical development to execute on biomarker strategies in clinical trials .Writing memos, final reports and publications summarizing data, and… more
    HireLifeScience (10/19/24)
    - Save Job - Related Jobs - Block Source
  • Genmab (Plainsboro, NJ)
    …for coordinating sourcing for new trials to ensure efficient and effective trial operations.Point of Contact for Global Clinical Trial Managers: Act ... of contact, facilitate communication and resolve issues.Vendor Owner:First Point of Contact for clinical trial vendors: Serves as the first point of contact for… more
    HireLifeScience (10/23/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (North Wales, PA)
    …Management, and other company Research Laboratories Scientists in designing and analyzing clinical trials , and in coordinating the statistical activities for ... other potential problems arising in the design, conduct, and analysis of clinical trials , proposes solutions and carries them out.Develops individual protocols… more
    HireLifeScience (11/06/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (Rahway, NJ)
    …and monitor performance across our portfolio, studies & processes within Global Clinical Trial Operations (GCTO).Primary responsibilities include but are not ... or health care related discipline.Required Experience and Skills:At least 8 years working on a clinical trial team or has worked in a clinical operations… more
    HireLifeScience (11/12/24)
    - Save Job - Related Jobs - Block Source
  • Genmab (Plainsboro, NJ)
    …Perform ongoing surveillance (including signal detection/evaluation) of safety data from Genmab clinical trials . Be the primary safety contact for other ... review and input to various documents including but not limited to: Trial Protocols, eCRFs/CRFs, and TMFs. Contribute to the development of other documentation… more
    HireLifeScience (11/15/24)
    - Save Job - Related Jobs - Block Source
  • Eclaro (Mercerville, NJ)
    …and analytics teams. Qualifications: Strong understanding of data sources, such as clinical trial data, electronic health records, and other healthcare ... then take a chance at this rewarding opportunity! Position Overview: Clinical Safety Analytics Associate will play a critical role within the PV CoE. This… more
    JobGet (11/18/24)
    - Save Job - Related Jobs - Block Source
  • Novo Nordisk Inc. (Plainsboro, NJ)
    …the application of those principles to trial design, planning & conduct of clinical trials Advanced capability in MS Excel, MS PowerPoint and MS Word ... experience with Supplier Management, Research Administration, Grant Operations, Grant Management, clinical trial management, or a similar research operations… more
    HireLifeScience (11/08/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (North Wales, PA)
    …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life… more
    HireLifeScience (09/27/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (North Wales, PA)
    …Engineering or related field plus 9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life ... field plus 7 or more years SAS programming experience in a clinical trial environmentDepartment Required Skills and Experience: Excellent interpersonal skills… more
    HireLifeScience (11/12/24)
    - Save Job - Related Jobs - Block Source
  • Genmab (Plainsboro, NJ)
    …and/or leading a small team to complete various programming efforts within a clinical trial .You will be responsible for ensuring integrity, consistency, and ... essential to fulfilling our purpose.The Role & Department As a Senior Programming Associate or Programming Manager, you will be in the Statistical Programming team… more
    HireLifeScience (10/11/24)
    - Save Job - Related Jobs - Block Source
  • Novo Nordisk Inc. (Plainsboro, NJ)
    …actual product Responsible for all areas related to patient safety in clinical trials Act as member of the trial safety group for dose escalation decisions ... (phase I trials ) Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator's Brochure (IB),… more
    HireLifeScience (09/13/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (North Wales, PA)
    …of 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment.MS (preferred) in Computer Science, Statistics, Applied ... of 7 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. Required-Experience and Skills: Proven track record for… more
    HireLifeScience (11/07/24)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (Rahway, NJ)
    …new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide...in relevant discipline.-Knowledge and Skills:--Minimum 6 years' experience in Clinical Data Management or Pharmacovigilance as appropriate to business… more
    HireLifeScience (11/16/24)
    - Save Job - Related Jobs - Block Source
  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …preferred Experience- 7 or More Years Outsourcing, health sciences or related field ( clinical trials ) required- 7 or More Years Deep experience in pharma ... & category management required- CRO experience preferred- Strong knowledge of clinical trials preferred- Demonstrated ability to leverage digital data… more
    HireLifeScience (09/24/24)
    - Save Job - Related Jobs - Block Source