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In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.

At Amgen, we believe in a “biology first” approach. We use cutting-edge science and technology to study the subtlest biological mechanisms in search of therapies that will improve the lives of those who suffer from serious diseases. Amgen believes the cure for disease can be found inside each and every one of us.

Amgen

Senior Medical Science Liaison - Cardiovascular Metabolic - Central Pennsylvania

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Write all 'non-science' grant sections, including facilities and resource descriptions, human subject's protection, project management, data security, organizational capabilities, budget justifications, draft letters of support, etc. The Departmental Research Administration team in Anesthesiology and Critical Care Medicine (CAA) is looking for a new Grants Coordinator to help expand the support for our research investigators and department, both in Pre- and Post-Award.

YEAR

Children's Hospital of Philadelphia

Senior Grants Coordinator - Anesthesiology and Critical Care Medicine

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Responsibilities: • Leads or plays a key role in cross-functional teams for the review of safety data or safety-related reports • Mentors and trains newer members of the functional area • Ensures functions to comply with national and international regulations, such as GxP guidelines and/or any other relevant international and national legislation(s), regulations(s), and guidance(s) as well as company policies and procedures in area of responsibility • Ensures direct reports to support and ensure QPPV's oversight on the company's Pharmacovigilance system, and identify, implement and monitor KPIs/KQIs across the company and manages cross functional CAPAs and other improvement activities on behalf of the QPPV. • Participate in ICSR reporting compliance analysis and respective CAPA • Together with Risk Management function develops and maintains Medical Concepts to support internal decision making and safety analyses for safety surveillance and provides expertise to pharmacovigilance and clinical development programs with regards to safety data/ SAE coding • Manages regular MedDRA upgrades and provides impact analysis to RM physicians and ME • Develop and provide advanced analytical outputs to global teams to support analyses and decision making based on safety data.

CSL Behring LLC

Senior Clinical Trial Case Manager

Position Summary: The Team Lead, Therapeutic Area Quality (GCP / Clinical Quality) is responsible for leading a team of Quality Business Partners who provide independent GCP (Good Clinical Practice) quality oversight and expert support to key stakeholders across clinical trial conduct and R&D programs. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.

GSK plc

Senior Director Team Lead, Therapeutic Area Quality (GCP / Clinical Quality)

Collaborate with the Clinical organization to enhance patient enrollment in Phathom-sponsored clinical trials by identifying appropriate trial sites and interacting with investigators in ongoing studies. MSLs provide medical information through scientific exchange in a fair-balanced manner and provide clinical/scientific support for Phathom and the Medical Affairs department at the direction of Medical Affairs management.

Phathom Pharmaceuticals, Inc

Medical Science Liaison/Senior Medical Science Liaison (Msl) - PA & Upstate NY

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FULL_TIME

Proficiency in Excel, Word, Power Point, and other software skills; Excellent written/verbal communication skills; Strong interpersonal skills, presentation, and teaching skills; Ability to work independently and in a team structure; Ability to adjust effectively to work within new structures, processes, requirements, or cultures; Strong planning and organizational skills; team and leadership skills. Combined with strong strategic vision, market therapeutic area awareness, as well as clinical expertise, the MSL/Senior MSL serve as a conduit of information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized by AbbVie.

AbbVie

MSL/Senior Oncology, Multiple Myeloma (Mid-Atlantic)

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Proficiency in Excel, Word, Power Point, and other software skills; Excellent written/verbal communication skills; Strong interpersonal skills, presentation, and teaching skills; Ability to work independently and in a team structure; Ability to adjust effectively to work within new structures, processes, requirements, or cultures; Strong planning and organizational skills; team and leadership skills. Present scientific information and education relative to disease state, therapeutic landscape, and AbbVie products across the product lifecycle to healthcare professionals including physicians, academic institutions, researchers, and other health care professionals.

MSL/Senior MSL, Parkinson's Disease (Great Lakes)

MSL/Senior MSL Oncology, Multiple Myeloma (Upstate NY/Alleghany)

The Medical Director will be responsible for collaborating with clinical operations, regulatory, translational medicine/biomarkers, clinical pharmacology, CMC, and quality assurance functions; liaising with clinical investigators and site personnel; and establishing and building relationships with key external experts. Any resumes submitted without an agreement and/or any resumes sent unsolicited through e-mail accounts of Avalo employees will be considered outside of the appropriate process, do not imply or create any obligation on our part, do not impart any restrictions on Avalo with respect to the hiring of any persons whose resumes are so submitted and are not eligible for placement fees.

Avalo Therapeutics

Medical Director/Sr. Medical Director, Clinical Development- Rheumatology

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Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process. Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality.

Madrigal Pharmaceuticals

Vice President, Clinical Development Program Leader

What You Will Bring: Required for the Role: Bachelor's degree Human Resources, Organizational Development, Industrial/Organizational Psychology, Business Administration, Higher Education Administration, Law, Social Work, Counseling or a related field. Demonstrated experience leading HR operations, including HR service delivery, HRIS and data (Workday or comparable), process design, and the operational infrastructure that keeps the function running day to day.

Bucknell University

Chief Human Resources Officer

Madrigal Pharmaceuticals Inc

Working across assigned products and therapeutic areas, the Director partners with Medical Affairs operational counterparts and Global Development/Post Approval Delivery Unit teams to translate evidence-generation strategy into the compliant clinical and operational implementation of Company Sponsored Studies (CSS), Investigator Initiated Studies (IIS), Collaborative Studies, and other post-marketing research conducted through insourced, outsourced, or matrixed organizations. Budgeting, Clinical Trials, Clinical Trials Operations, Coaching, Compliance Management, Contract Management, Developing Others, Execution Focus, Fact-Based Decision Making, Give Feedback, Inclusive Leadership, Laboratory Operations, Leadership, Process Improvements, Project Integration Management, Research and Development, Research Ethics, Technical Credibility

Caring for the world, one person at a time... inspires and unites the people of Johnson&nbsp;&amp;&nbsp;Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson&nbsp;&amp;&nbsp;Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

Our Family of Companies comprises:

 The world’s sixth-largest consumer health company. 
 The world’s most comprehensive medical devices business. 
 The world’s sixth-largest biologics company. 
 And the world’s fifth-largest pharmaceuticals company. 


We have more than 265 operating companies in more than 60 countries employing approximately 126,500 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

Johnson & Johnson

Director, Clinical Operations, Immunology

Drawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.

Senior Investigator Jobs in Pennsylvania

Senior Medical Science Liaison - Cardiovascular Metabolic - Central Pennsylvania Amgen

Senior Grants Coordinator - Anesthesiology and Critical Care Medicine Children's Hospital of Philadelphia

Senior Clinical Trial Case Manager CSL Behring LLC

Senior Director Team Lead, Therapeutic Area Quality (GCP / Clinical Quality) GSK plc

Medical Science Liaison/Senior Medical Science Liaison (Msl) - PA & Upstate NY Phathom Pharmaceuticals, Inc

MSL/Senior Oncology, Multiple Myeloma (Mid-Atlantic) AbbVie

MSL/Senior MSL, Parkinson's Disease (Great Lakes) AbbVie

MSL/Senior MSL Oncology, Multiple Myeloma (Upstate NY/Alleghany) AbbVie

Medical Director/Sr. Medical Director, Clinical Development- Rheumatology Avalo Therapeutics

Vice President, Clinical Development Program Leader Madrigal Pharmaceuticals

Chief Human Resources Officer Bucknell University

Vice President, Clinical Development Program Leader Madrigal Pharmaceuticals Inc

Director, Clinical Operations, Immunology Johnson & Johnson

Associate Medical Director Apothecom

Director, Clinical Operations, Immunology 6120-Janssen Scientific Affairs Legal Entity

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