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Randstad Senior Clinical Research Scientist in North Billerica, Massachusetts

Senior Clinical Research Scientist

job details:

  • location:North Billerica, MA

  • salary:$140,000 - $145,000 per year

  • date posted:Tuesday, January 12, 2021

  • experience:5 Years

  • job type:Permanent

  • industry:Professional, Scientific, and Technical Services

  • reference:34674

job description

Senior Clinical Research Scientist

job summary:

As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: North Billerica, Massachusetts

job type: Permanent

salary: $140,000 - 145,000 per year

work hours: 9 to 5

education: Doctorate

responsibilities:

The Clinical Research Scientist (CRS) contributes to the design, data collection, data review and reporting of clinical studies. This position has a key role in support of clinical development.

  • Responsible for the relevance and accuracy of clinical science planning and guidance for a clinical study (e.g., study concepts/synopsis, eligibility, database elements, protocol and product-related training, investigative site questions, literature benchmarks) to clinical study teams

  • Works closely with internal and external stakeholders to accumulate scientific and clinical knowledge necessary to support clinical development execution of clinical protocols and data collection

  • Leads/reviews key product and study related documents and deliverables including study synopsis, clinical protocols/amendments, study manuals, Investigator's Brochures, informed consent forms, Case Report Forms, Clinical Study Reports, Annual Reports, Statistical Analysis Plans, and regulatory submissions

  • Works with investigative sites and/or study teams to answer protocol related questions, resolve study conduct issues

  • Prepare and may present protocol designs, clinical data and other information at advisory boards, investigator meetings, site initiations and other internal and external settings

  • Reviews clinical data listings, patient profiles and summaries to ensure data collection proceeds in a manner consistent with the protocol and strategic objectives.

  • Assists the project team in the monitoring and analysis of emerging data trends.

  • Participates in review and management of safety reports and submissions

  • Participate in clinical and safety database reconciliation

  • Support the development of clinical sections for regulatory correspondence and submissions including but not limited to Information Requests, Meeting Information Packages and presentation materials, and IND/NDAs

  • Contribute to authoring and design of study-related documents and deliverables, including but not limited to Clinical Protocols, Investigator Brochures, Study Manuals, Case Report Forms, Clinical Study Reports, Annual Reports, , regulatory submissions and abstracts.

  • Supports project team with conduct of clinical studies including clinical trials registration and results reporting, and in the monitoring and analysis of emerging clinical data and safety data trends. May be consulted in data management deliverables, clinical monitoring activities, interim analyses planning and Data Safety Monitoring Board or Steering Committee meetings as applicable.

  • Interacts with internal and external stakeholders (Key Opinion Leaders, Medical Director, vendors, committees) in support of clinical trial objectives and deliverables, including investigator-sponsored trials.

  • Conducts literature reviews to support clinical development programs and regulatory submissions.

  • Attends scientific meetings to remain abreast of clinical developments, interact with investigators, and advisors

qualifications:

  • An MD, PharmD or PhD is required, a Master's degree will be considered with additional experience

  • Candidates should have a minimum of 5+ years experience in clinical research development.

  • Oncology experience

  • Industry experience

  • Has authored industry documents and/or has published in medical/scientific peer-reviewed journals.

  • Has medical writing and data management/analysis experience

  • Understanding of GCP/ICH

  • Must possess highly effective analytical, communication (verbal and written), and presentation skills

  • Proficient in MS Office Suite and have the ability to multi-task and work effectively in a team or independently on assigned tasks.

  • Demonstrated problem solving and sound decision-making skills

  • Ability to be well organized, detail oriented, and flexible

  • Must be able to work productively in an extremely fast-paced collaborative environment;

  • Adaptable to multiple demands, shifting priorities, and be agile to operate at-risk based on available supported information

skills: IND, NDA, Clinical research, MS-WORD, MS-EXCEL, MS-Powerpoint, GCP (Good Clinical Practice), Submissions, ICH Regulations

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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