Clinical Trial Assistant – Clinovo – Tucson, AZ

Clinovo’s mission is to empower healthcare and life science companies by providing expertise sourcing and placing top clinical research professionals across a multitude of diverse opportunities. We have a proven track record with pharmaceutical, biotechnology, diagnostic, medical device, and CRO customers. Leading companies have chosen Clinovo as their preferred partner for its quality of customer service, excellent candidate pro?le, and its long-term relationships. We are currently searching for a Clinical Trial Assistant.

CONTRACT OPPORTUNITY FOR ONE YEAR WITH POSSIBILITY OF EXTENSION

LOCATION: TUCSON, ARIZONA

POSITION : CLINICAL TRIAL ASSISTANT

Duties

1. Trial Master Files / Site Trial files: Work with study teams to identify TMF requirements and developing, maintaining, and archiving trial documentation in accordance with related SOPs working under minimal oversight.

2. Clinical Trial Materials / Binders / Labels: Work with study teams to identify specifications and develop study related materials to those specifications working under minimal oversight. May also assist in the maintenance and periodic review of

3. Receiving: Receives, inspects and inventories Clinical Trial Supplies ensuring appropriate quality, quantities and storage conditions of materials / supplies, completing relevant documentation as necessary, and communications with Clinical Teams.

4. Picking / Packing / Shipping: Follows moderate to complex instructions from Clinical Team to fill shipping requests of Clinical Trial Supplies and/or Samples ensuring accuracy of items and quantities, appropriate packing materials and shipping conditions (e.g., frozen, refrigerated and ambient), as well as shipping instructions to ensure compliance with all DOT, IATA, and local and federal regulations.

5. Establish good working relationships across all Life Cycles and Facilities groups to effectively deliver work objectives.

6. Accurately and effectively communicate needs, issues, and project status with manager, Clinical Teams, Warehouse and Shipping staff.

7. Performs additional duties as requested by manager or designee.

Skills

1. Able to communicate clearly and accurately both written and spoken in English

2. Experience working as part of a team

3. Self-motivated and displays initiative

4. General knowledge of medical/scientific terminology and ICH/GCP guidelines

5. Detail oriented

6. Experience using copying / printing equipment

7. Experience using various computer applications including spreadsheets, email and word-processing software

This is a one-year contract opportunity with the possibility of extension

Job Types: Full-time, Contract

Pay: $22.00 – $27.00 per hour

Schedule:

• Monday to Friday

Ability to commute/relocate:

• Tucson, AZ: Reliably commute or planning to relocate before starting work (Preferred)

Application Question(s):

• Do you have experience working with Trial Master Files(clinical trials)?

Education:

• High school or equivalent (Preferred)

Experience:

• Clinical trials: 1 year (Preferred)

Work Location:

• One location

Work Remotely:

Work Location: One location