Senior Medical Writer - Cardio/Metabolic Health & Regulatory
ProPharma
ProPharma in Raleigh, North Carolina, seeks a skilled medical writer with at least 5 years of experience. The role involves authoring a variety of clinical and regulatory documents while ensuring adherence to regulatory standards. The ideal candidate will demonstrate strong project management abilities and a deep understanding of clinical research principles. ProPharma values diversity and encourages innovative thinking in a collaborative environment. #J-18808-Ljbffr ProPharma
- ..., ProPharma has improved the health and wellness of patients by providing... ...that empowers biotech, medical device, and pharmaceutical... ...With deep domain expertise in regulatory sciences, clinical research solutions... ...less experienced medical writers, as necessary. Adhere to...SeniorRegulatoryContract work
- Syneos Health/inVentiv Health Commercial LLC is looking for a Medical Writer in North Carolina. This role involves leading medical writing deliverables, managing activities... ...clinical studies, and ensuring compliance with regulatory standards. The ideal candidate should have 3-5...SeniorRegulatory
$333.3k
The Senior Medical Director, Clinical Development, will play a key role... ...within the Cardiovascular/Renal/Metabolism portfolio focused on obesity... ...strategies and subsequent regulatory submissions. This role... ...filings and interactions with health authorities preferred This...SeniorRegulatoryLocal area$245.6k
...Therapeutic Area Head, Cardio Metabolic and Intensive Care Syneos Health® is a leading fully integrated... ...unique clinical, medical affairs and commercial... ...Responsibilities The Senior Vice President (SVP),... ...with client C-suites, regulatory stakeholders, and industry...RegulatoryFlexible hours- Syneos Health, Inc. is seeking a Senior Medical Writer in Morrisville, NC, to lead and execute comprehensive medical writing deliverables. This role is... ...emphasizes coordination across departments to meet regulatory standards. The ideal candidate will have 3-5 years of...SeniorRegulatory
- Sr Medical Writer Publications - Sponsor Dedicated - Remote Based Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate... ...scientific meetings. Adheres to established regulatory standards, including, but not limited to, ICH...SeniorRegulatoryRemote jobContract workFlexible hours
- ...solutions organization is seeking a Sr Medical Writer. The role involves leading the completion... ...studies, and ensuring compliance with regulatory standards. Candidates should possess... ...ability to mentor others. Benefits include health insurance, 401k matching, and more....SeniorRegulatoryRemote job
- ProPharma seeks an experienced Medical Writer in Raleigh, NC, to author and manage medical writing deliverables across clinical research... ...candidate will have at least 5 years of experience in clinical or regulatory writing and a Bachelor's degree in a medical or scientific...SeniorRegulatoryRemote job
$62k - $108.6k
Principal/Sr Medical Editor - Regulatory Documents - Copy Editing + QC - NA/Canada Remote Based Syneos Health is a leading fully integrated biopharmaceutical solutions organization... ...projects and updates the lead medical writer, project manager, and/or direct supervisor...SeniorRegulatoryRemote jobContract workFlexible hours- ## Senior Clinical Research Associate - CNS/Rare Disease - Midwest - RemoteApplyremote... ...therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare... ...you'll receive extensive support through regulatory submissions, TMF management, and in-house...SeniorRegulatoryWork at officeRemote workWorldwide
- ...Grifols is seeking a Clinical Research Associate to manage clinical monitoring processes and ensure regulatory compliance. You will track study tasks, conduct monitoring visits, and facilitate investigator site interactions to support clinical trials. The ideal candidate...SeniorRegulatory
- ...Syneos Health, Inc. is seeking a Principal Medical Writer to lead the development and finalization of medical documents for clinical studies and regulatory submissions. The role involves collaborating with clinical and medical teams to ensure clarity and compliance. Key...Regulatory
$38.51 - $58.82 per hour
...nursing care. The role includes leading clinical practice, promoting education and development for staff, and ensuring compliance with regulatory standards. Applicants must hold a BSN, be licensed to practice as a Registered Nurse in North Carolina, and have 18 months of...SeniorRegulatoryHourly payFull timeNight shift$62k - $108.6k
...biopharmaceutical solutions organization seeks a Principal/Sr Medical Editor to manage editorial responsibilities for regulatory documents. The candidate will ensure compliance... ...2,000 to $108,600, along with benefits including health coverage and paid time off. Ideal for someone...SeniorRegulatoryRemote job- PruittHealth is seeking a Senior Nurse Consultant for their Rapid Response Team to support long-term care centers in regulatory compliance. This role includes conducting mock surveys, identifying risks, and facilitating quality improvement initiatives. The ideal candidate...SeniorRegulatory
- ...LLC is seeking a Clinical Data Manager to lead data management activities for complex clinical studies, ensuring compliance with regulatory standards and overseeing database implementations. The role requires a strong understanding of data management timelines, collaboration...SeniorRegulatory
- ...ICON Clinical Research is looking for a Senior Clinical Research Associate in Raleigh, North Carolina. You will oversee clinical trial activities to ensure they are aligned with protocol and regulatory standards. Responsibilities include monitoring trial sites, conducting...SeniorRegulatory
$333.3k
Regeneron Pharmaceuticals, Inc is seeking a Senior Medical Director for Clinical Development to guide clinical development programs in the Cardiovascular/Renal/Metabolism portfolio. This role involves leading clinical team interactions, developing innovative strategies...Senior$80.6k - $145k
...Morrisville, NC is seeking an experienced Medical Writer to ensure the accurate completion of... ...complex writing projects, adhering to regulatory standards, and mentoring junior writers... ...and quality reviews. Benefits include health insurance, car allowance, and a competitive...SeniorRegulatory- ...trials from start to finish, ensuring adherence to protocols and regulatory guidelines. Responsibilities include preparing and submitting... ...strong communication and organizational skills. We provide medical benefits, paid time off, and a rewarding work environment. #J...SeniorRegulatory
- Senior Manager, Clinical Data Management Department... ...need, with a focus on metabolic disorders, neurology,... ...quality, integrity, and regulatory compliance throughout... ...operations, biostatistics, medical monitoring, regulatory... ...in life sciences, health informatics, computer...SeniorRegulatoryFull timeTemporary workWork at officeHome officeFlexible hours
- Syneos Health/ inVentiv Health Commercial LLC is seeking a senior digital creative leader to drive the creative strategy across clinical trial marketing. The role... ...teams, enhancing patient engagement, and ensuring regulatory compliance. Candidates should have strong...SeniorRegulatory
- MMS Holdings Inc is looking for a Senior Biostatistician in Raleigh, North Carolina. This role involves creating randomization schedules... .... The position includes collaboration with clients and regulatory bodies while ensuring compliance with ICH guidelines. Strong communication...SeniorRegulatory
- ...plans, supervising the care team, and ensuring compliance with regulatory standards. Ideal candidates will have an RN license, strong... ...effectively with all stakeholders. Join our team and make a positive impact in the lives of seniors! #J-18808-Ljbffr The HermitageSeniorRegulatory
- ...North Carolina, is seeking a skilled professional to conduct programming tasks on large RWE projects suitable for publication and regulatory review. The role requires proficiency in SQL and SAS, along with experience in data visualization and EHR data utilization. The...SeniorRegulatory
- Description # Implements health and safety programs aligned with the organizational safety management system. # Implements ISO 14... ...coordination with external consultants. # Manages site activities with regulatory agencies to verify compliance, resolve situations, and maintain...SeniorRegulatoryLocal areaImmediate start
- Job Description Seeking a highly experienced Senior Consultant with deep expertise in EDI (Electronic Data Interchange), specifically... ...resolve EDI-related issues, ensuring compliance with HIPAA and other regulatory standards. Maintain documentation and support onboarding of new...SeniorRegulatoryDay shift
$18.5 - $42.35 per hour
We ’re building a world of health around every individual — shaping a more... ...Under general supervision the Senior Document Writer drafts, reviews, and edits medical, dental and vision plan documents... ...understanding of compliance and regulatory issues (ERISA, HIPAA, ACA, COBRA...SeniorRegulatoryHourly payFull timeTemporary workWork at officeLocal area- ...stages of the clinical study, including identification of potential sites, study start-up activities such as collecting appropriate regulatory documents, and supporting negotiation of contracts and budgets. Training sites to collect data properly and report any potential...SeniorRegulatoryWork at officeRemote workWorldwide
- ...development projects. The ideal candidate will have a Master's Degree in Life Sciences and a strong understanding of clinical trials and regulatory submissions. This role involves coordinating data, writing clinical documents, and ensuring effective communication across...SeniorRegulatory
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