Medical Affairs Associate

Job not on LinkedIn

🔥 21 hours ago

🏄 California – Remote

🏄 California – Remote

💵 $36 / hour

⏳ Contract/Temporary

🟡 Mid-level

👻 Ghost score 23%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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DAWAR CONSULTING INC

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2009

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

DAWAR CONSULTING INC. is a trusted provider of workforce solutions and professional services tailored for the Medical Science industry. Specializing in Human Capital Management (HCM) and ITSM consulting, DAWAR offers expert implementation of SaaS and Cloud-based solutions from platforms like Workday and ServiceNow. Their comprehensive staffing services include global talent acquisition, recruitment process outsourcing, and staff augmentation, ensuring that they connect skilled professionals with career opportunities while enhancing organizational productivity and efficiency.

📋 Description

• Support clinical trials from study start-up through closeout • Coordinate Expanded Access Programs, OOS cases, and Single-Patient IND activities • Review and maintain essential clinical study documents, including protocols, ICFs, IBs, and CRFs • Coordinate CROs, vendors, investigators, and clinical trial sites • Track enrollment, screening, data flow, protocol deviations, milestones, and study deliverables • Support site feasibility, investigator meetings, site communications, and training • Monitor program risks, resolve operational issues, and escalate concerns • Prepare study metrics, status reports, newsletters, and management updates • Support clinical data queries and database lock activities • Ensure compliance with applicable regulations and procedures

🎯 Requirements

• Bachelor's degree in Nursing, Life Sciences, or a related healthcare field • 3–5 years of Clinical Operations / Clinical Trial experience • Familiarity with CTMS, EDC, and clinical trial documentation • Strong organizational, communication, and problem-solving skills • Ability to manage multiple priorities in a fast-paced environment • Oncology or Hematology clinical trial experience (preferred) • Cellular therapy experience (preferred) • iMedidata / RAVE EDC experience (preferred) • Study start-up experience in a CRO, sponsor, or site-based regulatory environment (preferred) • Exposure to transplant patient care or apheresis collection (preferred)

🏖️ Benefits

• Medical • Paid sick leave (as per state policy) • Possibility of contract extension

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