Current jobs related to Senior Clinical Research Associate 1 - Jurong East - Labcorp
-
Clinical Research Associate
3 days ago
East Coast, Singapore Abiomed Full timeAbiomed, part of Johnson & Johnson MedTech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives. Abiomed’s “Patients First!” culture drives our skilled workforce and strong relationships with clinicians. Our innovative product portfolio and robust pipeline provide...
-
Clinical Research Associate
5 days ago
East Coast, Singapore Abiomed Full timeAbiomed is a pioneer and global leader in healthcare technology and innovation, with a mission of **Recovering Hearts & Saving Lives**. With corporate headquarters in Danvers, Massachusetts, offices in Aachen & Berlin, Germany and Tokyo, Japan, Abiomed’s 1,400 employees form one of the fastest growing medical device companies in the world. We attract and...
-
Clinical Research Associate Ii
1 week ago
Jurong East, Singapore Labcorp Full timeThe Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a Local Project...
-
In-house Cra I
2 weeks ago
Jurong East, Singapore Labcorp Full time**Essential Job Duties**: - To serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites. - To monitor site performance and implement action plans for sites not...
-
Clinical Research Associate Ii
5 days ago
Jurong East, Singapore Labcorp Full time**Essential Job Duties**: 1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. 2) Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of...
-
senior Executive/ Assistant Manager
2 weeks ago
Jurong East, Singapore Singapore Chinese Chamber of Commerce & Industry Full time**Senior Executive/ Assistant Manager (Research & Advocacy)**: **Responsibilities** - To actively undertake practical research and analysis on economic and business issues (e.g., enterprise capability building, manpower, business cost, internationalization, government assistance schemes, etc.) with a view to offer evidence-based recommendations and...
-
Clinical Research Associate Ii
2 hours ago
Jurong East, Singapore Labcorp Full timeEssential Job Duties: 1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. 2) Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study...
-
Senior Executive(Clinical Governance)
2 hours ago
North-East Singapore Emprego SG Full time**Location** Singapore, North East **Job Type** Permanent **Salary** $2,500 - $5,000 Per Month **Date Posted** 23 minutes ago Additional Details **Job ID** 13661 **Job Views** 1 Roles & Responsibilities The incumbent will be responsible for the following: - Organise and provide secretariat support to clinical quality assurance committees,...
-
Fitness Associate
7 days ago
Jurong East, Singapore Buddhist Compassion Relief Tzu-Chi Foundation (Singapore) Full timeConduct one-on-one fitness assessments and consultations with senior members to understand their individual health and fitness goals, limitations, and preferences. Design personalized fitness programs tailored to the specific needs and abilities of senior members, incorporating elements of strength training, cardiovascular exercises, flexibility, and balance...
-
Associate Clinical Project Manager
1 week ago
Jurong, Singapore Nestlé Full time**Position Snapshot** Location: Singapore Company: Nestle R&D Center, Singapore Type of contract: Permanent **Position Summary** Joining Nestlé means you are joining the largest Food and Beverage Company in the world. At our very core, we are a human environment - passionate people driven by the purpose of enhancing the quality of life and contributing...
Senior Clinical Research Associate 1
3 weeks ago
**Essential Job Duties**:
1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties.
2) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
3) Responsible for all aspects of site management as prescribed in the project plans
4) General On-Site Monitoring Responsibilities:
5) Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
6) Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
7) Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review
8) Monitor data for missing or implausible data
9) Ensure the resources of the Sponsor and Labcorp are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Labcorp travel policy
10) Ensure audit readiness at the site level
11) Travel, including air travel, may be required and is an essential function of the job.
12) Prepare accurate and timely trip reports
13) Manage small projects under direction of a Project Manager/Director as assigned a. Serve as lead monitor for a protocol or project, and may assist in establishing monitoring plans and trip report review as assigned
14) Review progress of projects and initiate appropriate actions to achieve target objectives
15) Organize and make presentations at Investigator Meetings
16) Participate in the development of protocols and Case Report Forms as assigned
17) Participate in writing clinical trial reports as assigned
18) Interact with internal work groups to evaluate needs, resources and timelines
19) Act as contact for clinical trial supplies and other suppliers (vendors) as assigned
20) Responsible for all aspects of registry management as prescribed in the project plans
21) Undertake feasibility work when requested
22) Conduct, report and follow-up on Quality Control (QC) visits when requested
23) Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned
24) Negotiate study budgets with potential investigators and assist the Labcorp legal department with statements of agreements as assigned
25) Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
26) Independently perform CRF review; query generation and resolution against established data review guidelines on Labcorp or client data management systems as assigned by management
27) Assist with training, mentoring and development of new employees, e.g. co-monitoring
28) Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned
29) Perform other duties as assigned by management
**Experience**:
- Minimum Required:_
- Two (2) years of Clinical Monitoring experience
- Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
- Advanced site monitoring skills - Advanced study site management skills
- Advanced registry administration skills - Ability to work with mínimal supervision
- Good planning and organization skills
- Good computer skills with good working knowledge of a range of computer packages
- Advanced verbal and written communication skills
- Ability to train and supervise junior staff
- Ability to resolve project-related problems and prioritizes workload for self and team - Ability to work within a project team
- Works efficiently and effectively in a matrix environment
- Valid Driver's License
- Preferred:_
- One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
- Local project coordination and/or project management experience
**Education/Qualifications**
- Minimum Required: _
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
- Thorough knowledge of regulatory requirements
- Thorough understanding of the drug development process
- Fluent in local office language and in English, both written and verbal
- Or an equivalent combination of education and ex
