- Visit customers' houses to conduct site measurements for cabinets, wardrobes, and other related products.
5 days
19 Clinical Study Assistant Jobs - October 2026 - Urgent Hiring
Showing 19 jobs results for
"clinical study assistant"
Part-Time Clinical Study Assistant
- Approach eligible participants, explain the clinical study, and obtain their informed consent.
9 days
Part-Time Clinical Study Assistant
9 days
Clinical Study Assistant | Pharma MNC | Office Hours #HVN
- Key Responsibilities:
8 days
Clinical Study Assistant | Pharma MNC | Office Hours #HVN
- Key Responsibilities:
14 days
Contract Clinical Study Assistant | Pharma MNC | Office Hours #HVN
- Key Responsibilities:
12 days
Contract Clinical Study Assistant | Pharma MNC | Office Hours #HVN
- Provide administrative and coordination support for clinical studies
16 days
Contract Clinical Study Assistant | Pharma MNC | Office Hours #HVN
- Key Responsibilities:
19 days
Clinical Study Assistant (Long-Term Part Time $14, hrly ) #HCK
- Location: Buona Vista, Singapore
22 days
Contract Clinical Study Assistant (Pharm MNC) - Up to $3K| Office Hours | West #HHL
- Assist with trial documentation, study file organization, and data entry/verification.
19 days
Contract Clinical Study Assistant | US Pharma MNC | 5 Days Office Hours #HCT
- Looking to build your career in Clinical Research with a reputable US Pharmaceutical MNC?
23 days
Clinical Project Assistant (PERM) #HRY
- Support the project manager and the clinical team on project related tasks:
12 days
CRA I-CRA II-Sr CRA
- Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings
17 days
Clinical Research Assistant
23 days
Clinical Project Assistant (Training provided)l - HTJ
- Assist the clinical team with updating and maintaining clinical systems that track study & site compliance and performance within project timelines.
24 days
Clinical Project Assistant (Training provided) - HTJ
- Assist the clinical team with updating and maintaining clinical systems that track study & site compliance and performance within project timelines.
26 days
Clinical Project Assistant (Training provided)l - HTJ
- Assist the clinical team with updating and maintaining clinical systems that track study & site compliance and performance within project timelines.
28 days
CRA I-CRA II-Sr CRA
- Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings
30+ days
Clinical Project Admin Assistant (Biotech) #HRY
- Job ScopeConduct pre-study, site initiation, routine monitoring and close-out visits in accordance with ICH-GCP, ClinActis SOPs and client requirements.
26 days