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WC

WEP Clinical

via Lever.co

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Site Management Associate

Anywhere
full-time
Posted 11/20/2025
Direct Apply
Key Skills:
Flexible
Team Player
Detail Oriented
Highly Organized
Effective Verbal And Written Communication Skills
Strong Organizational Skills
Attention To Detail
Computer Literacy
Proficiency In Microsoft Office
Clinical Systems
Ability To Handle Confidential Information
Willingness To Travel

Compensation

Salary Range

$Not specified

Responsibilities

The Site Management Associate is responsible for supporting and managing clinical trial sites through start-up, conduct, and closeout activities. This role ensures compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements while maintaining strong relationships with investigators and site staff.

Requirements

A Bachelor's Degree in a health or science field is preferred, along with 2+ years of experience in site management or clinical research. Candidates should possess strong organizational skills, attention to detail, and effective communication skills.

Full Description

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives. Role Objectives: The WEP Clinical Site Management Associate is responsible for supporting an managing clinical trial sites through start-up, conduct and closeout activities. The SMA ensures compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements while maintaining strong relationships with investigators and site staff to support efficient study execution. \n Ideal Candidate: Flexible Team Player Detail Oriented Highly Organized What You'll Do: Collaborate with Clinical Operations to develop site initiation timelines and ensure adherence to project milestones. Prepare and manage site startup documentation, including contracts, informed consent forms, and regulatory submissions. Coordinate with contracts and budget teams to ensure timely execution of site agreements. Assist with the preparation and submission of essential regulatory documents for site activation. Ensure all documents are approved by ethics committees and IRBs before site activation. Track progress of regulatory submissions, site contracts, and essential document collection. Verify site readiness with adequate resources and completed training prior to patient enrolment. Participate in study kick-off and initiation meetings to align expectations and timelines. Troubleshoot activation issues and escalate problems to the Project Manager or CRA when needed. Assist with the setup of study supplies and equipment at the site, including investigational products and lab kits. What You'll Need: Bachelor's Degree (in a health or science field preferred) 2+ years’ experience in site management, clinical research, or equivalent combination of education, experience, and expertise Computer literacy and proficiency in Microsoft Office and clinical systems (e.g., EDC,CTMS, eTMF) Effective verbal and written communication skills Ability to handle confidential information with complete discretion Strong organizational skills and attention to detail Ability and willingness to travel up to 20% of the time \n What We Offer: Medical, dental, and vision insurance, FSA, HSA Voluntary short-term and long-term disability insurance Voluntary life insurance 401K safe harbor plan and company match Paid vacation, holiday, and sick time Paid maternity & paternity leave What sets us apart: WEP Clinical partners with sponsors to help patients and physicians gain early access to medicines when no other treatment options are available. WEP Clinical has over 15 years of experience distributing products to over 120 countries worldwide to treat unmet patient needs. We're Committed to Our Team: WEP has many initiatives to encourage wellness, growth and development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events, and all that we do to support our employees. We're Committed to DEI: At WEP Clinical, acceptance, recognition, and engagement are the core of our DEI values. We are committed to giving employees opportunities for personal and professional success and growth, embracing everyone's unique identities. Our services include: Access Programs Clinical Trial Services Patient Site Solutions Clinical Trial Supply Market Access and Commercialization WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment. WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.

This job posting was last updated on 11/26/2025

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