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Become A Senior Clinical Scientist

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Working As A Senior Clinical Scientist

  • Getting Information
  • Analyzing Data or Information
  • Identifying Objects, Actions, and Events
  • Updating and Using Relevant Knowledge
  • Documenting/Recording Information
  • Mostly Sitting

  • $117,490

    Average Salary

What Does A Senior Clinical Scientist Do At Abbvie

* Executes clinical Pharmacokinetics/Pharmacodynamics (PK/PD) research or development that achieves project and therapeutic area goals.
* Understands PK/PD regulatory advances, strengths, weaknesses, opportunities, and threats and assists with responses and appropriate new strategies.
* Acts as a lead Pharmacokineticist on one or more studies and investigates, identifies, develops, and optimizes new PK/PD models.
* Develops productive collaborations and communications with other groups, across multiple disciplines.
* Utilizes PK/PD expertise to provide PK/PD consultation to the business and leadership on decisions and development plans for multiple projects within a therapeutic area.
* Develop productive collaborations and communications with other groups across multiple disciplines.
* Writes, communicates, presents PK/PD materials.
* Contributes to the development of commercial and regulatory strategies by formulating PK/PD plans including development activities.
* Assists in the development of PK/PD plans to satisfy regulatory expectations and defend plans and interpretation of data to management.
* Integrates knowledge of all aspects of development from Discovery through Phase 4 (exposure, safety, efficacy, formulation, regulatory impact).
* Primary contributor to PK/PD interpretations of reports for regulatory filings and clinical protocols.
* Contributes to interpretation of study-related projects for external publications, project reviews, reports and/or regulatory submissions.
* Author in peer-reviewed journals, R&D reports, and/or regulatory documents/filings.
* May contribute to due diligence

What Does A Senior Clinical Scientist Do At Abbott

* Design, develop, and write clinical protocols, reports and publications.
* Develop physician relationships with experts in the cardiovascular (specifically, heart valve medical device) field.
* Well developed, advanced knowledge and skills in an applied research area of their specialization.
* Incumbents require an understanding of a number of disciplines (e.g. trial design, statistical methods, results analysis, medical writing, strategic evidence planning, creating scientific presentations).
* Position may involve the introduction and application of new developments in their field and may also require the development of new approaches to be used by other professions.
* Prepare detailed reports to support recommendations and conclusions and evaluate findings.
* Provides information essential to estimate the costs, resources, and time required to implement the organization’s annual clinical goals and monitor the performance of clinical research projects to ensure targets are met.
* Frequently liaises with the external scientific community

What Does A Senior Clinical Scientist Do At Xencor

* 13; ---Create required clinical trial documents including clinical protocols, investigator brochures, DSURs and clinical modules of the IND
* Work closely with Clinical Operations to execute the clinical trial with high quality and according to timelines
* Perform ongoing review of clinical data, query generation/resolution and data analysis, including review of draft listings to support data cleaning and interpretation
* Provide scientific expertise to Clinical Operations by responding to questions or clarifying issues arising during study conduct
* Provide internal safety monitoring for clinical trials
* Provide medical input for the clinical database build, CRFs, monitoring plan, data management plan, and statistical analysis plan
* Develop and maintain relationships with clinical trial investigators and therapeutic area key opinion leaders
* Lead review of study data (e.g.
* Tables, Listings and Figures and emerging bioanalytical data) and development of CSRs, clinical presentations and publications
* Support other members of Clinical Development and Regulatory Affairs departments as may be required
* Participates as a standing member of multidiscipline Project Teams Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job.
* Duties, responsibilities and activities may change at any time with or without notice.

What Does A Senior Clinical Scientist Do At Medimmune

* The Clinical Scientist will work under the supervision of the Medical/Clinical Research personnel (Clinical Leader, Medical Director, or Senior Clinical Scientist) to assist in the preparation of INDs, Clinical Development Plans (CDPs), protocols, and Clinical Study Reports (CSRs), and the execution of clinical trials.
* The Clinical Scientist may serve in various roles including membership on a clinical team and clinical project sub-teams, may serve in leadership roles within these teams, and may be a representative on the Product Development Team (PDT).
* Responsibilities
* Performing medical data review to ensure integrity and credible study data:
* Blinded Safety Review
* Serious Adverse Events (SAEs)
* Physical Exam, Medical history and concomitant medication
* Council for International Organizations of Medical Sciences (CIOMS) Review
* Narrative Reviews
* Protocol Deviation reviews
* Coding reviews
* Assist in the creation and maintenance of the CDP for assigned programs ensuring alignment with the Target Product Profile (TPP), taking into account feasibility and regional requirements, capturing health outcomes, epidemiology, and pharmacogenetic considerations.
* Assist the Medical/Clinical Research personnel to:
* Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports.
* Develop and review key documents to support the components of a regulatory submission (i.e. IND Annual reports, Briefing book for pediatric investigational plan)
* Review and interpret study results as appropriate (i.e. after CSR is final, provide results to study investigators, etc).
* Prepare clinical publications or provide input into communication and publication development
* Become familiar with the latest thinking regarding mechanism of disease, diagnostic tests, treatment, drug development trends, and regulatory requirements in assigned disease and therapeutic areas.
* Internal Collaboration:
* Assist the Medical/Clinical Research personnel to:
* Establish links between company experts in relevant departments, including regulatory, bio-pharmaceutics, discovery, and pharmacology/toxicology sciences, to initiate and expedite clinical studies.
* Collaborate with translational science to optimize approach to study target neutralization and understand mechanism of action.
* Coordinate with pharmacovigilance personnel in developing the Benefit Risk Management Plan in conjunction with Medimmune’s Safety Monitoring Committee and other external groups as appropriate.
* Collaborate with R&D and other senior management stakeholders to assess requirements for emerging products.
* Collaborate with Sales and Marketing to enhance Medimmune’s commercial efforts and design clinical research studies with maximum marketplace credibility.
* External Collaboration:
* Assist with the management of and input into Scientific Advisory Boards convened to develop CDP strategies as appropriate.
* Assist in conducting efforts to obtain external scientific and clinical validation of clinical research protocols.
* Assist in establishing links with outside experts to initiate and expedite clinical studies.
* May include seeking advice from key external experts, regulatory, pricing/reimbursement, and market access experts.
* Operations
* May participate in the tactical execution of the clinical development protocols by providing guidance, input, and implementation support as appropriate.
* This may include:
* Study Management Plans.
* Contract and financial oversight of assigned projects.
* Review study budgets and expenses, ensure study related contractual and budgeting issues are upheld and performed.
* Outsourcing strategy within the clinical project team and recommending service providers.
* Activities of CROs and other vendors.
* Identification and selection of clinical research centers and investigators.
* Assist with contract negotiations when necessary.
* Investigator meetings, advisory boards and other scientific committees as required by the protocol (e.g.
* Independent reviews, Data Safety Monitoring Boards, etc.).
* Study risk mitigation and highlight of potential issues and solutions.
* Training of internal team members and investigative sites to ensure protocol and GCP requirements are met.
* Ensuring that study level activities/resources are aligned to allow implementation of the study protocol in a manner consistent with the current plan/timeline and CDP

What Does A Senior Clinical Scientist Do At Inova Health Systems

* Provide leadership in developing and conducting ethics consultation services for high volume Ethics Consultation Service
* Provide leadership to develop, implement, maintain and evaluate ethics orientation, education and outreach programs
* Provide support for the Ethics Committee and assume responsibility for subcommittee meetings
* Provide multidisciplinary education in the undergraduate and graduate medical curricula
* Conduct independent and collaborative ethics research and scholarship
* Assure compliance with regulatory and accreditation standards pertaining to clinical ethics and patient rights

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How To Become A Senior Clinical Scientist

Medical scientists typically have a Ph.D., usually in biology or a related life science. Some medical scientists get a medical degree instead of a Ph.D., but prefer doing research to practicing as a physician.

Education

Students planning careers as medical scientists typically pursue a bachelor’s degree in biology, chemistry, or a related field. Undergraduate students benefit from taking a broad range of classes, including life sciences, physical sciences, and math. Students also typically take courses that develop communication and writing skills, because they must learn to write grants effectively and publish research findings.

After students have completed their undergraduate studies, they typically enter Ph.D. programs. Dual-degree programs are available that pair a Ph.D. with a range of specialized medical degrees. A few degree programs that are commonly paired with Ph.D. studies are Medical Doctor (M.D.), Doctor of Dental Surgery (D.D.S.), Doctor of Dental Medicine (D.M.D.), and Doctor of Osteopathic Medicine (D.O.). Whereas Ph.D. studies focus on research methods, such as project design and data interpretation, students in dual-degree programs learn both the clinical skills needed to be a physician and the research skills needed to be a scientist.

Graduate programs emphasize both laboratory work and original research. These programs offer prospective medical scientists the opportunity to develop their experiments and, sometimes, to supervise undergraduates. Ph.D. programs culminate in a thesis that the candidate presents before a committee of professors. Students may specialize in a particular field, such as gerontology, neurology, or cancer.

Those who go to medical school spend most of the first 2 years in labs and classrooms, taking courses such as anatomy, biochemistry, physiology, pharmacology, psychology, microbiology, pathology, medical ethics, and medical law. They also learn how to record medical histories, examine patients, and diagnose illnesses. They may be required to participate in residency programs, meeting the same requirements that physicians and surgeons have to fulfill.

Medical scientists often continue their education with postdoctoral work. Postdoctoral work provides additional and more independent lab experience, including experience in specific processes and techniques such as gene splicing, which is transferable to other research projects.

Licenses, Certifications, and Registrations

Medical scientists primarily conduct research and typically do not need licenses or certifications. However, those who administer drugs, gene therapy, or otherwise practice medicine on patients in clinical trials or a private practice need a license to practice as a physician.

Important Qualities

Communication skills. Communication is critical, because medical scientists must be able to explain their conclusions. In addition, medical scientists write grant proposals, because grants often are required to fund their research.

Critical-thinking skills. Medical scientists must use their expertise to determine the best method for solving a specific research question.

Data-analysis skills. Medical scientists use statistical techniques, so that they can properly quantify and analyze health research questions.

Decisionmaking skills. Medical scientists must determine what research questions to ask, how best to investigate the questions, and what data will best answer the questions.

Observation skills. Medical scientists conduct experiments that require precise observation of samples and other health data. Any mistake could lead to inconclusive or misleading results.

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Senior Clinical Scientist jobs

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Senior Clinical Scientist Demographics

Gender

  • Female

    61.1%
  • Male

    34.6%
  • Unknown

    4.3%

Ethnicity

  • White

    75.1%
  • Asian

    13.3%
  • Hispanic or Latino

    8.7%
  • Unknown

    2.1%
  • Black or African American

    0.8%
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Languages Spoken

  • Spanish

    37.5%
  • Chinese

    12.5%
  • Irish

    6.3%
  • Sicilian

    6.3%
  • German

    6.3%
  • Japanese

    6.3%
  • French

    6.3%
  • Mandarin

    6.3%
  • Korean

    6.3%
  • Italian

    6.3%
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Senior Clinical Scientist

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Real Senior Clinical Scientist Salaries

Job Title Company Location Start Date Salary
SR. Clinical Scientist Medical Science & Computing, LLC Bethesda, MD Dec 20, 2014 $155,998
Senior Clinical Physicist Johns Hopkins University Baltimore, MD Oct 01, 2015 $151,722
Senior Clinical Pharmacokinetcist I Abbvie Inc. North Chicago, IL Mar 09, 2016 $147,434
SR. Clinical Scientist Medical Science & Computing, Inc. Bethesda, MD Apr 04, 2013 $142,800
SR. Clinical Scientist Medical Science & Computing, Inc. Bethesda, MD Apr 04, 2011 $140,000
Associate Medical Director/Sr. Clinical Scientist Seattle Genetics, Inc. Bothell, WA Sep 05, 2013 $130,000 -
$160,000
Senior Clinical Pharmacokineticist Abbvie Inc. North Chicago, IL Jun 13, 2016 $126,582
Senior Clinical Affairs Scientist Perrigo Pharmaceuticals Company Piscataway, NJ Nov 08, 2013 $125,368
Senior Clinical Affairs Scientist Perrigo Pharmaceuticals Company NJ Nov 05, 2014 $125,368
Senior Clinical Affairs Scientist Perrigo Pharmaceuticals Company Piscataway, NJ Nov 05, 2014 $125,368
Senior Clinical Affairs Scientist Perrigo Pharmaceuticals Company NJ Sep 15, 2015 $125,368
Senior Clinical Affairs Scientist Perrigo Pharmaceuticals Company Allegan, MI Nov 08, 2013 $125,368
Senior Clinical Pharmacokineticist II Abbvie Inc. North Chicago, IL Dec 21, 2015 $125,000
Senior Clinical Scientist Philips Electronics North America Corporation Baltimore, MD Sep 02, 2015 $125,000
Senior Clinical Pharmacokineticist I Abbvie Inc. North Chicago, IL Oct 01, 2015 $123,497
Senior Clinical Pharmacokineticist I Abbvie Inc. North Chicago, IL Jul 22, 2015 $120,246
Senior Clinical Pharmacokineticist Abbvie Inc. North Chicago, IL Mar 23, 2016 $120,000 -
$123,000
Senior Clinical Pharmacokineticist II Abbvie Inc. North Chicago, IL Jul 22, 2016 $120,000
Senior Clinical Pharmacokineticist I Abbvie Inc. North Chicago, IL Jul 22, 2015 $120,000
Senior Clinical Pharmacokineticist I Abbvie Inc. Redwood City, CA Jun 04, 2016 $120,000
Senior Clinical Pharmacokineticist II Abbvie Inc. North Chicago, IL Nov 17, 2014 $120,000
SR. Clinical Pharmacokineticist Abbvie Inc. North Chicago, IL Sep 09, 2013 $119,383
Senior Manager, Clinical Pharmacology Scientist Tesaro, Inc. Waltham, MA Jan 05, 2015 $115,000 -
$145,000
Senior Clinical Pharmacokineticist II Abbvie Inc. North Chicago, IL Nov 04, 2016 $115,000 -
$120,000
Senior Clinical Affairs Scientist Perrigo Pharmaceuticals Company Piscataway, NJ Nov 08, 2010 $112,000
Senior Clinical Pharmacokineticist Abbvie Inc. North Chicago, IL Mar 09, 2016 $110,000
Senior Clinical Pharmacokineticist I Abbvie Inc. North Chicago, IL Aug 20, 2015 $110,000
Senior Clinical Pharmacokineticist I Abbvie Inc. North Chicago, IL Apr 07, 2014 $110,000
Senior Clinical Pharmacokineticist I Abbvie Inc. North Chicago, IL Aug 28, 2014 $110,000

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Top Skills for A Senior Clinical Scientist

SafetyRegulatorySubmissionsClinicalProtocolsOccupationalTherapyFDACrosClinicalTrialsInvestigatorBrochuresStudyProtocolsPhaseIIIOncologyINDCRAFullCaseloadClinicalStudyReportsTreatmentPlansAdverseEventsPatientCareSAEIV

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Top Senior Clinical Scientist Skills

  1. Safety
  2. Regulatory Submissions
  3. Clinical Protocols
You can check out examples of real life uses of top skills on resumes here:
  • Performed ongoing review of study database to identify potential safety issues.
  • Key contributor to regulatory submissions, FDA advisory committee meetings and publications.
  • Provided Occupational Therapy services in the Acute Care setting under direct supervision of a licensed supervisor.
  • Prepared materials and attended FDA Advisory Committee meeting.
  • Reinforced nursing's role in health promotion, health maintenance, and disease prevention across the lifespan among vulnerable populations.

Top Senior Clinical Scientist Employers

Senior Clinical Scientist Videos

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A day in the life of a Biomedical Engineer - Chapter 2

A day in the life of a Biomedical Engineer - Chapter 3

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