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clinical research in Boston

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  1. Senior Medical Writer

      Regulatory Medical Writer Must have written all of the following: NDA submissions, Protocols, Narratives, Case Report Studies, and Inform Consent forms   Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical ...

  2. Clinical Writer / Scientist

    Our client in the Chelmsford area is seeking a Clinical Scientist.  You will work under supervision of Vice President for Clinical Affairs and other senior clinical leaders  in the research and writing of clinical briefings, white papers and research articles.  Writing will contribute to company strategy as well as web and print publications. Qualifications   Credentials and Experience:   The ideal candidate will have clinical training in medicine, nursing or pharmacy.  Experience in clinical ...

  3. 30813 – Sr. Clinical Trials Specialist

    This Senior Clinical Operations Specialist is responsible for managing the oversight and implementation of biomarker strategic objectives.   Responsibilities include budget and contract management, sample quality, timeliness and biomarker administrative needs (budget, presentations and study documents). This role is responsible for all budget and contract management related to biomarker related research agreements, 2 or 3 way collaborations, material transfer agreements, collaborative studies ...

  4. 94530 Sr. Associate, Regulatory Affairs

    Job Description: Responsible for ex-US Clinical Trial Application (CTA) submissions to national competent authorities (to include initial submissions, amendments, notifications and report), the level of support to vary depending on whether a CRO or affiliate is performing the submission. Analysis of regulatory issues and guidelines related to clinical trials. Responsible for accuracy and content of submissions and communications with regulatory bodies. Responsible for supporting efforts to comply ...

  5. VP of Quality

    For details and to apply, please visit http://www.careervitals.com/j/6782523 Job Title: VP of Quality Company Name: MMS Group Location: Boston, Massachusetts Job Type: Full-Time Profession: Other Career Level: Experienced Experience: 10-15 years Education Level: Bachelors Degree Job Details: VP of Quality Improvement - Growing health plan !Innovative organization continues to be a strong leader in managed care nationwide and is growing once again in New England. As the ...

  6. Sr. Regulatory Affairs Associate II

    We have a Contract opportunity with a prominent client for a Senior Associate II, Regulatory Affairs  in Cambridge, MA.   Description:   *Must possess exceptional communication skills (both written and verbal) *Will be required to communicate with all levels within the organization   Job Title: Senior Associate II, Regulatory Affairs  Responsible for ex-US Clinical Trial Application (CTA) submissions to national competent authorities (to include initial submissions, amendments, notifications ...

  7. Scientist I, Biochemistry & Bioanalytics - 105046

    Scientist I – 9 month contract We are seeking to fill a contract position in Biochemistry and Bioanalytics group to contribute to the early stage oncology drug discovery research in Sanofi. The successful candidate will involve the biological sample preparation and consequential analysis of molecules ranging from small molecule to proteome with advanced mass spectrometers to identify clinically translatable biomarkers and understand cell signaling network and mechanism of actions. The primary ...

  8. Clinical Trial Specialist (Contract)

    Clinical Trial Specialist (Contract)   Responsibilities: Conduct and facilitate specific start-up activities such as feasibility, site identification, pre-qualification, Site Regulatory Package (SRP) review and approval, Clinical Site Agreements (CSA) and Informed Consent (ICF) customization and negotiation (where required). IRB/IEC application preparation and submission, in accordance with relevant regulations, SOPs and study specific procedures.   Qualifications: Min 1 year of experience with ...

  9. 3887653 – Scientist I

      We are seeking to fill a contract position in Biochemistry and Bioanalytics group to contribute to the early stage oncology drug discovery research.   Responsibilities:   The successful candidate will be involved with the biological sample preparation and consequential analysis of molecules ranging from small molecule to proteome with advanced mass spectrometers to identify clinically translatable biomarkers and understand cell signaling network and mechanism of actions The primary ...

  10. Scientist I - (Biochemistry & Bioanalytics)

    Contract is approved until the end of the year (12/31/2014). Contracts with this company are reviewed at that time, and often extended.   Job Title :          Scientist I   Duties:  We are seeking to fill a contract position in Biochemistry and Bioanalytics group to contribute to the early stage oncology drug discovery research in Sanofi. The successful candidate will involve the biological sample preparation and consequential analysis of molecules ranging from small molecule to proteome with ...

  11. Sr. Medical Science Liaison - Raleigh

    For details and to apply, please visit http://www.careervitals.com/j/6782393 Job Title: Sr. Medical Science Liaison - Raleigh Company Name: William Halderson Associates, Inc. Location: Raleigh, North Carolina Job Type: Full-Time Profession: Scientist Career Level: Experienced Experience: 5-10 years Education Level: Doctorate Travel: 75% Job Details: Position Title: Sr. Medical Science LiaisonPosition Reports To: Director, Medical AffairsBase Location:Raleigh, covering NC, ...

  12. Sr. Medical Science Liaison - Los Angeles

    For details and to apply, please visit http://www.careervitals.com/j/6782392 Job Title: Sr. Medical Science Liaison - Los Angeles Company Name: William Halderson Associates, Inc. Location: Los Angeles, California Job Type: Full-Time Profession: Scientist Career Level: Experienced Experience: 5-10 years Education Level: Doctorate Travel: 75% Job Details: Position Title: Sr. Medical Science LiaisonPosition Reports To: Director, Medical AffairsBase Location:Los Angeles, ...

  13. Sr. Medical Science Liaison - Denver

    For details and to apply, please visit http://www.careervitals.com/j/6782391 Job Title: Sr. Medical Science Liaison - Denver Company Name: William Halderson Associates, Inc. Location: Denver, Colorado Job Type: Full-Time Profession: Scientist Career Level: Experienced Experience: 5-10 years Education Level: Doctorate Travel: 75% Job Details: Position Title: Sr. Medical Science LiaisonPosition Reports To: Director, Medical AffairsBase Location:Denver, covering CO, UT, NV, ...

  14. Sr. Medical Science Liaison - St. Louis

    For details and to apply, please visit http://www.careervitals.com/j/6782390 Job Title: Sr. Medical Science Liaison - St. Louis Company Name: William Halderson Associates, Inc. Location: St. Louis, Missouri Job Type: Full-Time Profession: Scientist Career Level: Experienced Experience: 5-10 years Education Level: Doctorate Travel: 75% Job Details: Position Title: Sr. Medical Science LiaisonPosition Reports To: Director, Medical AffairsBase Location:St. Louis, covering IN, ...

  15. Sr. Medical Science Liaison - Cleveland

    For details and to apply, please visit http://www.careervitals.com/j/6782389 Job Title: Sr. Medical Science Liaison - Cleveland Company Name: William Halderson Associates, Inc. Location: Cleveland, Ohio Job Type: Full-Time Profession: Scientist Career Level: Experienced Experience: 5-10 years Education Level: Doctorate Travel: 75% Job Details: Position Title: Sr. Medical Science LiaisonPosition Reports To: Director, Medical AffairsBase Location:Cleveland, covering OH, MI, ...

  16. Sr. Medical Science Liaison - Dallas

    For details and to apply, please visit http://www.careervitals.com/j/6782388 Job Title: Sr. Medical Science Liaison - Dallas Company Name: William Halderson Associates, Inc. Location: Dallas, Texas Job Type: Full-Time Profession: Scientist Career Level: Experienced Experience: 5-10 years Education Level: Doctorate Travel: 75% Job Details: Position Title: Sr. Medical Science LiaisonPosition Reports To: Director, Medical AffairsBase Location:Dallas, covering TX, OK, AR, and ...

  17. Sr. Medical Science Liaison - Boston

    For details and to apply, please visit http://www.careervitals.com/j/6782387 Job Title: Sr. Medical Science Liaison - Boston Company Name: William Halderson Associates, Inc. Location: Boston, Massachusetts Job Type: Full-Time Profession: Scientist Career Level: Experienced Experience: 5-10 years Education Level: Doctorate Travel: 75% Job Details: Position Title: Sr. Medical Science LiaisonPosition Reports To: Director, Medical AffairsBase Location: Boston, covering New ...

  18. Manager Statistical Programming

     ~The Manager of Statistical Programming is responsible for the statistical programming aspects of projects for clients and project teams through management of internal staff. The Manager of Statistical Programming maintains optimal department processes, implements project-specific strategies, and assists with the development and implementation of department strategies to increase productivity and quality, while decreasing cycle times and costs. The Manager of Statistical Programming assists with the ...

  19. Sr Clinical Research Associate - Oncology

    We have a top CRO client who is looking for a full time Sr CRA with Oncology experience anywhere in New Hampshire   Requirements/Qualifications:   ·         Registered Nurse certification and/or a Bachelor’s degree in nursing, pharmacy, life sciences or a related health field, or equivalent experience in healthcare.   ·         Minimum of 3 to 5 years of related clinical trial experience with a pharmaceutical company or CRO; prior project management experience desired.   ·     Coordinates ...

  20. Sr Clinical Research Associate - Oncology

    We have a CRO client who is looking for a Full Time/Perm Sr CRA with Oncology experience in the Boston area   Requirements/Qualifications:   ·         Registered Nurse certification and/or a Bachelor’s degree in nursing, pharmacy, life sciences or a related health field, or equivalent experience in healthcare.   ·         Minimum of 3 to 5 years of related clinical trial experience with a pharmaceutical company or CRO; prior project management experience desired.   ·     Coordinates/oversees ...

  21. Regional CRA (Boston, and Los Angeles)

     RCRA's needed in Boston, New Hampshire, Los Angeles  Must have Oncology monitoring experience ~~Description: The Clinical Research Associate manages all aspects of site monitoring responsibilities for clinical trials according to Good Clinical Practices (GCPs), company SOPs, ICH guidelines and study protocols, including pre-study, initiation, interim and closeout visits. Responsibilities:  Assists with study start-up activities.  Prepares study manuals, informed consent documents, regulatory ...

  22. Clinical Administrative Assistant - Healthcare!! $38k

    This position is an entry level role for a recent grad hoping to begin a career in Healthcare Administration. The ideal candidate could be someone hoping to go to nursing or medical school in the next few years and is looking to gain experience or someone hoping to study Healthcare Administration. This position is working with one of the larger hospitals in Boston in one of their clinical departments.  Job Summary: Provides administrative support to physicians in their clinical practice, academic ...

  23. Regulatory Affairs Project Manager

      ~~Hawkins Point Partners has an immediate need on its Cambridge, Massachusetts team for a Regulatory Affairs Manager with recent experience supporting FDA Clinical Trial Application (CTA) submissions. This person will ensure initial trial submissions, amendments, notifications and reports from internal and CRO or affiliate submissions.  Strong knowledge of the pharmaceutical clinical process along with analysis of regulatory issues and guidelines related to clinical trials is a core position ...

  24. PK-PD Contract Research Manager - Boston, MA

    Seeking 5+ years experience in Bioanalytical Research leadership and solid track record in Project Management to oversee and coordinate multiple CRO's on various PK-PD projects for global company. Shall: *** Develop and manage project timelines. *** Facilitate project review meetings, presentations and reports. *** Source, evaluate, contract, supervise and audit CRO's. *** Review data collection, analysis and reporting. *** Support technical transfers. *** Administer infrastructure ...