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This may include assistance in the development of essential clinical trial documents such as protocols, ICF documents/amendments, CRF’s, CSR’s, and Investigator Brochures. Promote quality review of data with an emphasis on subject safety and eligibility, data integrity, trend identification, analysis and remediation, and identification of AEs/SAEs for medical review.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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ICF is seeking a Senior Environmental Planner and Project Manager to join our Southern California based planning team to be based in our San Diego office, with the option for hybrid or full-time remote within San Diego County.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Provide operational and strategic input into study planning and study specific documents such as synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plan, Clinical Database edit specifications, Clinical Study Report (CSR) development, etc.
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The ICF Natural Resources practice is currently seeking a full time Principal Biologist and Project Manager with education and experience in biology, environmental impact analysis, regulatory compliance (ESA, Clean Water Act, State species and water statutes), planning, and project management to support our HCP, ESA, and CEQA/NEPA work.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Since 1969, public and private sector clients have worked with ICF to navigate change and shape the future. ICF is a global advisory and technology services provider, but were not your typical consultants.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Experience in running a trial from start to finish; initiating the trial that includes protocol development, ICF generation, site feasibility/start up training, contract and budget negotiation, vendor management, CRF design, maintaining a trial and study close out.
$150,000 - $165,000 a yearFull-timeExpandUpdated 2 months ago - UpvoteDownvoteShare Job
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We operate nine (9) ICF-DD-H residential facilities across San Diego County, and we need your expertise to make a difference in the lives of those we serve. We operate nine (9) ICF-DD-H residential facilities across San Diego County, and we need your expertise to make a difference in the lives of those we serve.
$45 - $50 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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We combine unmatched expertise with cutting-edge technology to help clients solve their most complex challenges, navigate change, and shape the future. We are an equal opportunity employer, committed to hiring regardless of any protected characteristic, such as race, ethnicity, national origin, color, sex, gender identity/expression, sexual orientation, religion, age, disability status, or military/veteran status.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Provide operational and strategic input into study documents such as synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plan, Clinical Database edit specifications, Clinical Study Report (CSR) development, etc.
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Demonstrated skills in writing and reviewing clinical study protocols, CRF, ICF and study documentation development, regulatory documents. ADARx has developed proprietary RNA targeting platforms and oligonucleotide delivery technologies for inhibition, degradation, and editing disease-causing mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system diseases.
$105,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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For more information, please read our EEO & AA policy (cf.com/legal/equal-employment-opportunity). We can only solve the world's toughest challenges by building an inclusive workplace that allows everyone to thrive.
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