Senior Clinical Trial Manager

Medasource; Pleasanton (CA); On-site; USD 140,000 - 175,000; Full time

Job summary

An established industry player is seeking a Clinical Trial Feasibility/Operations Consultant to join their dynamic team. This role involves collaborating with principal investigators and study teams to ensure the smooth initiation of clinical trials. The ideal candidate will possess a Bachelor's degree and demonstrate exceptional organizational and communication skills. In this fast-paced environment, you will tackle logistical challenges and contribute to groundbreaking clinical research. If you thrive in a collaborative setting and are passionate about advancing healthcare, this opportunity is perfect for you.

Benefits

Medical Insurance

Vision Insurance

Qualifications

• Bachelor's degree required; experience with clinical trials preferred.
• Excellent organizational and communication skills are essential.

Responsibilities

• Work with teams to determine study activities for clinical trials.
• Address logistical issues to launch clinical trials effectively.

Skills

Organizational Skills

Interpersonal Skills

Communication Skills

Experience with Clinical Trials

Familiarity with Medical Terminology

Education

Bachelor's Degree in a Related Field

Tools

Word Processing Software

Spreadsheet Software

Job description

2 days ago Be among the first 25 applicants

Title: Clinical Trial Feasibility/Operations Consultant

Start Date: ASAP

Location: Pleasanton, CA

Contract: 3 month Contract to Hire, M-F (40 hours/week)

The Clinical Trial Feasibility/Operations Consultant will work with a team under direct supervision of the Clinical Trials Operations Manager.

Responsibilities:

• Determine study activities related to clinical trial protocols.
• Work with principal investigators and study teams in clinical trial start up activities.
• Address logistical issues in order to launch clinical trials in medical facilities
• Must demonstrate excellent organizational, interpersonal, and communication skills
• Other duties as required to assist launching clinical trials.

Requirements:

• Bachelor's Degree in related field
• Must demonstrate excellent organizational, interpersonal, and communication skills.
• Experience with implementing/coordinating clinical trials
• Familiarity with medical terminology
• Must be able to work in a Labor/Management Partnership environment.
• Experience with word-processing and spreadsheet software programs

Soft Skills:

• Must be dependable, punctual, detail-oriented, and able to follow detailed protocols precisely.
• Experience with research administration.
• Must be able to work successfully with a wide variety of internal and external project staff and research participants
• Must exhibit a professional manner with a high degree of courtesy, tact, and sensitivity.
• Must be able to work well independently as well as part of a larger multi-disciplinary research team.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Other

• Industries

  Hospitals and Health Care

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Inferred from the description for this job

Medical insurance

Vision insurance

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