Entrada Therapeutics

Entrada Therapeutics

Clinical Scientist (CONSULTANT)

Boston, MA · Senior · Contract

Sponsorship not specified$44k-$601kDetected 7 days ago
GCPData AnalysisData VisualizationClinical TrialsCommunicationCollaborationProblem SolvingAdaptabilityBiostatistics

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odds of building a lasting career here

59Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds (Level IV)94
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~61% per draw at Level IV). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

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About the role

  • This individual will be highly motivated and experienced clinical researcher interested in working on all phases of clinical development.

Responsibilities

  • Support interpretation of clinical data to generate high quality summaries and insights to support regulatory filings, publications and scientific communications.
  • Consultant on the design of study-specific case report form (CRF) and author study-specific sections of the CRF completion guidelines, ensuring CRFs are aligned with study requirements during user acceptance testing.
  • Collaborate with Business Operations and Data Management to lead development and innovation of department clinical data technology access, retention, and visualization strategy, to support trend identification across programs.
  • Support innovation and strategy for the integration of new tools and technologies into phase 1-3 clinical studies.
  • Strong data analysis, data visualization and communication skills, with ability to write clear, accurate and concise documents, construct informative figures, and present to diverse audiences.

Requirements

  • You are a self-starter and an effective communicator.
  • You take accountability for known project responsibilities, but you can also easily adapt and accommodate the unexpected.
  • The right candidate will bring scientific rigor, deep expertise in clinical data review, and a passion for improving quality of life for patients and families impacted by rare neuromuscular disorders.

Nice to have

  • Experience in rare disease and/or neuromuscular disease is strongly preferred.

Compensation

  • $44k-$601k

Benefits

  • Collaborate cross-functionally with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Business Operations to help drive execution across clinical phases.
  • In partnership with Medical Directors, lead or support the authoring of selected sections of clinical study reports.
  • Support real-time data review, identify trends in safety and efficacy data and assessing protocol compliance including protocol deviation reviews, escalating to Medical Monitor(s) where appropriate.
  • Perform safety and efficacy reviews in preparation for DMC, in conjunction with Medical Director and other internal stakeholders, analyzing trends within and across programs.
  • Previous experience identifying trends and setting risk mitigation strategies in partnership with Medical teams within clinical studies.
  • Demonstrated history of creative problem-solving and learning ability.

Company info

  • Ph.D., PharmD, MD, Nursing, or Clinical Master's degree in a scientifically relevant field, with 6 + years of clinical development experience within the biotechnology or pharmaceutical industry.
  • Proven understanding of clinical development processes to serve as subject matter expert for phase 1-3 clinical studies.
  • Demonstrated experience in the design and execution of clinical trials and a strong understanding of GCP/ICH guidelines and regulatory expectations.
  • Skilled in Microsoft suite as well as innovative data review tools (ie. patient profiles, report generating tools)
  • Self-motivated, demonstrated success in delivering assigned tasks according to timelines.
  • Ability to interpret complex data and communicate clearly with both scientific and non-scientific stakeholders.
  • Desire to work in an innovative and collaborative, fast paced, mission driven environment, taking on new challenges with an adaptable mindset.
  • This is a US based remote, contract position with 40 hours per week expected, with preference given to local New England based candidates. This role will require a minimum quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA. #LI-Remote #LI-JF1
  • At Entrada, our passion for science, our devotion to patients and our values drives our behavior:
  • Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.

Equal opportunity

  • Entrada Therapeutics is an equal opportunity employer.
  • Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.
  • Third Party Staffing Agencies
  • Entrada does not accept unsolicited resumes from any source other than directly from candidates.

Visa & Work Authorization

  • rientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law
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This listing is sourced directly from Entrada Therapeutics's careers page and normalized into a canonical job model.