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Clinical documentation specialist [h1.location_city]

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Clinical documentation specialist • miami fl

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Senior Documentation Control Specialist

Senior Documentation Control Specialist

Summit Therapeutics Sub, Inc.Miami, FL, US
[job_card.full_time]
Location : On-Site 4 days per week at our Menlo Park, CA, Princeton, NJ or Miami FL locations.At Summit, we believe in building a team of world class professionals who are passionate about this miss...[show_more][last_updated.last_updated_variable_days]
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Clinical Quality Improvement Specialist

Clinical Quality Improvement Specialist

VITAS HealthcareMiami, FL, US
[job_card.full_time]
Performance Improvement Specialist.Performs ongoing quality assessment through data collection and analysis as directed by VITAS Policies, Procedures, and Standards. Works with hospice program leade...[show_more][last_updated.last_updated_variable_days]
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Clinical Documentation Specialist

Clinical Documentation Specialist

VirtualVocationsHialeah, Florida, United States
[job_card.full_time]
A company is looking for a Clinical Documentation Specialist Audit Coordinator (Remote).Key Responsibilities Provide clinical documentation integrity support and conduct audits of medical records...[show_more][last_updated.last_updated_1_day]
Clinical Simulation Specialist

Clinical Simulation Specialist

Miami Dade CollegeMiami, Florida, United States
[job_card.full_time] +1
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Become a Key Leader in MDC’s Simulation Hospital.Miami Dade College, Medical Campus | Simulation Hospital.Step into one of the nation’s most advanced academic Simulation Hospitals and help train th...[show_more][last_updated.last_updated_30]
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Clinical Sales Specialist (CS) - Kendall, FL

Clinical Sales Specialist (CS) - Kendall, FL

Corcept TherapeuticsMiami, FL, US
[job_card.full_time]
Clinical Sales Specialist (CS) - Kendall, FL.Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid recep...[show_more][last_updated.last_updated_variable_days]
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Loan Documentation Specialist

Loan Documentation Specialist

Pacific National BankMiami, FL, US
[job_card.full_time]
This individual is responsible for closing loans by engaging outside counsel or by preparing in-house documentation.Ability to read and interpret loan documentation and understand requirements cont...[show_more][last_updated.last_updated_variable_days]
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Clinical Pharmacy Specialist

Clinical Pharmacy Specialist

Larkin Community HospitalMiami, FL, US
[job_card.full_time]
Now Hiring : Pharmacy Clinical Specialist – Psychiatry.Advance Mental Health Care through Expert Pharmacy Practice.We are excited to announce a new opportunity to join our healthcare team as a...[show_more][last_updated.last_updated_30]
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Clinical Sleep Specialist - Orlando, Florida

Clinical Sleep Specialist - Orlando, Florida

ZOLL Medical CorporationMiami, FL, US
[job_card.full_time]
At ZOLL, we're passionate about improving patient outcomes and helping save lives.We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, softwar...[show_more][last_updated.last_updated_30]
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Respiratory Clinical Sales Specialist

Respiratory Clinical Sales Specialist

Sales OpeningsMiami, FL, US
[job_card.full_time]
If you have compassion and the passion for helping others, then we want you to join our growing team! Quipt Home Medical is a rapidly growing leader in the provision of clinical respiratory equipme...[show_more][last_updated.last_updated_30]
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Sr Clinical Specialist CRM Miami

Sr Clinical Specialist CRM Miami

MedtronicMiami, Florida, USA
[job_card.full_time]
We anticipate the application window for this opening will close on - 26 Jan 2026.At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare acces...[show_more][last_updated.last_updated_variable_days]
Documentation Specialist

Documentation Specialist

Tropical ShippingMiami
[job_card.full_time]
Responsible for shipment verification process from tally receipt until Bill of Lading has been issued.Maintains successive customer contact to expedite cargo movement from clear to load status, ens...[show_more][last_updated.last_updated_30]
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Documentation Associate

Documentation Associate

Banco de Credito e InversionesMiami, FL, US
[job_card.full_time]
Bci provides financial services to individuals and corporations.We focus on being a global leader in innovations and personalized client experience and, with more than 10,500 employees, Bci is reco...[show_more][last_updated.last_updated_variable_days]
EXPORT DOCUMENTATION 1

EXPORT DOCUMENTATION 1

GotWorx StaffingMiami, FL, United States
[job_card.full_time]
GotWorx Staffing seeks an experienced Export Coordinator.The duties for the position are as follows : .Reviewing documentation, dock receipts and invoices. Must have a strong understanding of export d...[show_more][last_updated.last_updated_variable_days]
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Clinical Business Operations Specialist

Clinical Business Operations Specialist

University of MiamiMiami, FL, US
[job_card.full_time]
Clinical Business Operations Specialist.The department of Medicine has an exciting opportunity for a full-time Clinical Business Operations Specialist to work onsite on the UHealth campus.The Clini...[show_more][last_updated.last_updated_30]
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Nurse Specialist - Center of Clinical Excellence

Nurse Specialist - Center of Clinical Excellence

The University of MiamiMiami, FL, United States
[job_card.part_time]
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a facu...[show_more][last_updated.last_updated_variable_days]
Sr. Clinical Specialist - Miami, FL

Sr. Clinical Specialist - Miami, FL

AbbottMiami, FL, United States
[job_card.full_time]
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. Career development with an international company where you can g...[show_more][last_updated.last_updated_variable_days]
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Clinical Documentation Improvement / Certified Professional Coder

Clinical Documentation Improvement / Certified Professional Coder

Palm Medical CentersMiami, FL, US
[job_card.full_time]
At Palm Medical Centers (PMC) our patients have the peace of mind knowing that their health and well-being are our primary concerns. We give our health plan clients the confidence that their members...[show_more][last_updated.last_updated_1_day]
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Clinical Sales Specialist II

Clinical Sales Specialist II

MasimoMiami, FL, US
[job_card.full_time]
The Clinical Specialist II is an advanced level position with a primary focus in large hospital systems.The Clinical Specialist II is responsible for supporting Masimo Products and maintaining cust...[show_more][last_updated.last_updated_1_day]
Senior Documentation Control Specialist

Senior Documentation Control Specialist

Summit Therapeutics Sub, Inc.Miami, FL, US
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  • [job_card.full_time]
[job_card.job_description]

Job Description

Job Description

Location : On-Site 4 days per week at our Menlo Park, CA, Princeton, NJ or Miami FL locations

About Summit :

Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit’s core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.

Summit’s team is inspired to touch and help change lives through Summit’s clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including :

Non-small Cell Lung Cancer (NSCLC)

  • HARMONi : Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
  • HARMONi-3 : Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
  • HARMONi-7 : Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)

  • HARMONi-GI3 : Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

    • Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China’s National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.

    Overview of Role :

    Reporting to the Director, Quality Systems, the Documentation Support Specialist will be supporting GxP operations at Summit. Reporting to the Director Quality Systems, the role encompasses a range of duties including the following :

  • ? Role and Responsibilities :
  • Support Quality team managing the electronic quality management documentation management system including uploading and archiving documents and handling associated requests
  • Delivers the ‘Service Owner’ role for the electronic Quality Management System to ensure the system is used by the wider organization and any error reporting is handled in an effective manner. Also ensures ongoing development and enhancement of the toolset to meet evolving business requirements.
  • Checks / maintains the compliance and quality of the documents, in relation to Standard(s), Guidance and Summit’s procedures and expectations
  • Responds to documentation enquiries, giving appropriate access to information
  • Supports other functions in drafting, reviewing and approving documents / records using the QMS
  • Supports the ongoing maintenance and improvement of standard operating procedures and user guides
  • Reports on progress of documents ensuring that documents are reviewed and approved within the review cycle
  • Supports in any other tasks as deemed appropriate by the Line Manager.
  • Support with QC checks for Regulatory and Safety team.

    • Experience, Education and Specialized Knowledge and Skills :

  • Minimum of 5 years of experience in a biotech or pharma industry.
  • Bachelor’s degree in science / life science related field and / or pharmaceutical sciences.
  • Must have excellent verbal and written communication skills.
  • Must be highly organized with a strong attention to detail.
  • Intermediate to advanced skills in MS Office Suite (Outlook, Excel, Word, PowerPoint).
  • Ability to work with minimal guidance; Proactive, motivated self-starter.
  • Understands pertinent regulations for the industry, for example, GLP, GCP, and 21 CFR Part 210, 211, and 820, ICH Guidelines, etc.
  • Minimum of two years in Quality Assurance in the Pharmaceutical / Biotechnology industry.
  • Experience in maintaining GXP training records, materials, or courses.

    • The pay range for this role is $97,000-$114,000 annually. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and / or other applicable variable compensation.

    Summit does not accept referrals from employment businesses and / or employment agencies in respect of the vacancies posted on this site. All employment businesses / agencies are required to contact Summit’s Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.