- Merck & Co. (Rahway, NJ)
- …tactical/scientific mentorship to other clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP and ICH) ... scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this.... , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data… more
- Merck & Co. (Rahway, NJ)
- …mentorship to other clinical scientists.Core Skills Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage ... SummaryThis position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the… more
- Merck & Co. (North Wales, PA)
- …managing any study specific partners and/or vendors.Core Skills: Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage ... DescriptionThis position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have… more
- Merck & Co. (North Wales, PA)
- …and key strategic engagements. This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability ... the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with key stakeholders within CSPV and external functions including Clinical Development, Research Development, Regulatory Affairs.Facilitate operational meetings ... language in associated contractual templates. Ensures Good Pharmacovigilance Practice and regulatory compliance in such arrangements. Contribute to the management of… more
- Genmab (NJ)
- …Writing Manager to help us tell the story of our science through compelling clinical and regulatory documents. You'll be at the heart of a team that plays ... Global Medical Writing team, you will drive the development of high-quality clinical documents to support operational, medical, and regulatory activities across… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The Programming Manager supports the development of new therapies by ensuring integrity, consistency and adherence ... the programming efforts of at least one study are in scope.The Programming Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical … more
- Merck & Co. (North Wales, PA)
- …Vice President in BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership and ... DescriptionIn Biostatistics and Research Decision Sciences (BARDS), a distinguished department within our renowned Research and Development division, quantitative… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions ... contact with key account personnel, including C-suite executives and department heads. Additionally, this role maintains relationships with other...NNI, a self-starter who is self-led and keeps their manager up to date on progress and ensures no… more
- Eisai, Inc (Nutley, NJ)
- …speakers and related aspects of speaker programsCollaborate with Promotional Program Manager for speaker usage and issuesOffer feedback on nominating new speakers ... of brand plansStrong communication and presentation skillsUnderstanding of legal and regulatory issues impacting pharmaceutical product marketing as well as the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable for ... technical and career, of direct reports, and mentors or acts as functional manager of skip-level or ex-US staff. This position requires strong knowledge about RBQM,… more
- Northwestern University (Chicago, IL)
- Department : MED-Physical Med & Rehab Salary/Grade: EXS/7 Target hiring range for this position will be between $62,000-$78,000 per year. Offered salary will be ... grants. Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) & all current local, state, & federal laws, regulations,… more
- Children's National Hospital (Washington, DC)
- The Clinical Research Program Manager will serve as a senior clinical research professional and is responsible for operational and financial management and ... day-to-day research program operations following Standard Operating Procedures (SOPs), Good Clinical Practices (GCP) and regulatory guidelines, company goals,… more
- Memorial Hermann Health System (Houston, TX)
- …or documented degree plan and timeframe to complete Bachelors Nursing For clinical manager positions in Magnet-designated hospitals or hospitals in pursuit ... Job Summary Position responsible for providing leadership to the department - overseeing the daily operations - managing and...(1) year experience in a supervisory or management role Clinical Manager II: additional two (2) years… more
- Eurofins (Tacoma, WA)
- …operation with corporate and regulatory policies and procedures. The Specialty Metals Department Manager will support the Business Unit Manager (BUMa) in ... Environment Testing in Tacoma,WA is seeking a Specilaity Metals Department Manager . The Specialty Metals Department...forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global… more
- OneOncology LLC (Alpharetta, GA)
- …in our community. Here, you'll find purpose in your work. Job Description: The Clinical Office Site Manager oversees the daily operations of a small oncology ... skills. Commitment to patient-centered care and continuous quality improvement. HIPAA Requirements The Clinical Office Site Manager will have access to PHI and… more
- Lifelancer (Boston, MA)
- About the job Clinical Trial Manager Job Title: Clinical Trial Manager Job Location: Boston, MA, USA Job Location Type: Remote Job Contract Type: ... managing clinical trial activities. Strong knowledge of ICH/GCP and regulatory requirements, with a strong preference for experience with EU-CTR. Strong… more
- Temple University (Philadelphia, PA)
- …a Clinical Research Nurse Manager to assist the Senior Director, Clinical Research Operations, the Regulatory team and liaise with the various hospital ... Clinical Research Nurse Manager The Lewis...Completing and tracking staff clinic assignments for the entire department Assisting Sr. Director, Clinical Research Operations… more
- Medpace, Inc. (Cincinnati, OH)
- …communicate/present both virtuall and face to face; and Support collaboration with Clinical Trial Manager other functional areas to provide study deliverables. ... Job Summary Our Clinical Packaging & Supplies team is growing rapidly,...opportunity for you. Responsibilities As a member of CP&S department , support and collaborate in all activities related to… more
- Kaiser Permanente (Vallejo, CA)
- Description: Job Summary: The Clinical Trial Nurse Manager (CTN- Manager ) position assists in the administrative leadership and direction of the operational ... budget, resource/allocation planning, and performance assessments for a variety of clinical , regulatory and research functions. Kaiser Permanente conducts… more
