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130000 Jobs (NOW HIRING)

Northern Bank

Commercial Loan Officer

Woburn, MA · On-site

$130K - $160K/yr

Proven track record of relationship/portfolio management as well as loan origination The salary range for this position is $130000 - $160000 per year About Northern Bank & Trust Company Northern Bank ...

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Senior Web Engineer (React)

Austin, TX · On-site +1

$130K - $180K/yr

Salary $130000 - $180000 * ~10+ employees * Seed Company * Skills: Node, React * H1B Transfer available Our Tech Stack * node.js * Typescript * AWS * Terraform * Postgres/Hasura * Docker * React ...

The Goodkind Group

Be Seen First

Tax Associate / Permanent

Rockville Centre, NY · On-site

$80K - $110K/yr

On-site, opportunity to work hybrid Salary: $80000= 130000 per year

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Clinical Research Associate II

Allen Spolden

Sacramento, CA

Other

Medical, Dental, Vision, Retirement

Posted 11 days ago

Job description

Job Title

Responsible for providing Clinical Research support for all clinical trials.

Job Information

Date Opened 09/19/2024

Job Type Full time

Industry Pharma/Biotech/Clinical Research

Work Experience 1-3 years

Salary 130000

City Sacramento

State/Province California

Country United States

Zip/Postal Code 94230

Job Description

Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of potential clinical sites according to established criteria of acceptability. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials. Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Prepare site visit reports with identification of key accomplishments, key issues for resolution and recommendations for follow-up actions for assigned study sites. Conduct study termination visits, obtain final reports from investigators, and participate in the preparation of final reports for regulatory submission. Assist with the maintenance of clinical archive and electronic files. Other tasks as assigned.

Requirements To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. BA, BS, RN, BSN or equivalent Basic knowledge and adherence to GCPs 1-2 years of clinical research experience or equivalent experience or training Strong attention to detail Ability to multi-task Unquestionable integrity and highest ethical standards Excellent written and verbal communication skills Self-motivated, assertive, and driven Benefits Dental, Medical, Vision and 401K

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