Clora’s Consultant Phenotypes

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Program Manager

  • Experienced lifecycle (Phase I ­ IV) program manager across several indications
  • Previously in management positions at Vertex, Biogen
  • Therapeutic areas: oncology, neurology, cystic fibrosis, inflammation, cardiovascular, metabolic disorders, multiple sclerosis

$125-150 / hr

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Clinical Project Manager

  • Accomplished global clinical manager with three decades of experience in Phase I ­ III project management and clinical quality.
  • Previously worked at Bausch and Lomb, Vertex, AstraZeneca, and Boston Scientific.
  • Therapeutic areas: hematology, oncology, ophthalmology, and autoimmune diseases.

$125-150 / hr

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Senior CRA

  • Over two decades of independent CRA experience for US and OUS trials. Served as lead CRA for 1000+ patient clinical trials.
  • Previously monitored phase I ­ IV studies for GSK, Genentech, Takeda, Hospira, Sanofi, and AstraZeneca.
  • Therapeutic areas: ophthalmology, oncology, musculoskeletal, nephrology (renal anemia), and endocrinology

$125-150 / hr

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Senior CRA

  • Senior CRA with over 15 years of experience in the CRO and biopharmaceutical space.
  • Previously monitored phase I ­ III studies for Roche, GSK, Sunesis, and PPD.
  • Therapeutic areas: hematology, oncology, infectious disease, and rheumatology.

$125-150 / hr

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Medical Writer

  • 20+ years of biopharma and device clinical and regulatory writing experience.
  • Previously worked at Pfizer, Sanofi, GSK, and BMS.
  • Well versed in protocol writing, CSRs, safety and efficacy summaries, regulatory documents for phase I-IV studies (including IND, NDA, and ICH guidelines) and clinical reviews.
  • Therapeutic areas: oncology, dermatology, gastroenterology, metabolic diseases amongst many others.

$125-150 / hr

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Medical Writer

  • 25+ years of expertise in writing, editing, strategic planning, and management services to support regulatory submissions. She has accelerated multiple INDs, NDAs and BLAs.
  • Previously worked on regulatory writing projects for Genentech, Covance, and Protein Design Labs.
  • Therapeutic areas: ophthalmology (AMD, autoimmune uveitis, Behçet disease, glaucoma, ocular hypotony, traumatic hyphema, vitreous hemorrhage, uveal melanoma), oncology, gastroenterology, cardiovascular, and vaccines.

$125-150 / hr

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CTA

  • 3 years of CTA experience with over 20 years of previous physical therapy experience.
  • Skilled at providing key administrative and quality control oversight of Phase I ­ III drug and device trials across nephrology, ophthalmology, and gastroenterology.

$125-150 / hr