Senior Biomarker Consent Specialist (Remote)

Jobgether•Kansas, KS

3d•Remote

About The Position

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Biomarker Consent Specialist - REMOTE. In this role, you will play a crucial part in advancing healthcare by negotiating, authoring, and reviewing essential genetic and biomarker language within clinical trial informed consent documents. As a proactive member of our dynamic team, you will have the opportunity to make impactful contributions to patient care while collaborating with multidisciplinary teams. Your expertise will help ensure compliance and consistency across international trials, directly facilitating the development of life-changing therapies for patients globally.

Requirements

Bachelor’s degree (BA/BS) required.
Minimum of 5 years of experience working with global clinical trials and associated systems (eTMF, LIMS, or similar).
Proven experience with genetic informed consents and global consent negotiation.
Exceptional communicator to partner effectively with internal and external teams.
Self-motivated professional who can work independently and collaboratively.
Critical thinker able to utilize and discern guidance documents as they apply to clinical trial informed consents.
Proactive problem solver to identify issues, propose solutions, and drive resolution.
Detail-oriented individual with the ability to manage multiple assignments under accelerated timelines.
Quick learner who can become proficient in client tools, databases, and systems.
Proficient MS Office Suite user.

Responsibilities

Author, review, and negotiate genetic and biomarker language within clinical trial informed consent documents.
Document restrictions related to genetic and biomarker research on clinical trial samples.
Understand and apply company policies and procedures to ensure consistency and compliance in informed consent language.
Collaborate with global stakeholders to negotiate informed consents across multiple regions.
Utilize clinical trial systems (eTMF, LIMS, etc.) to support documentation and workflow needs.
Manage multiple concurrent assignments while meeting accelerated project timelines.
Provide clear communication and partnership to cross-functional teams to achieve study and organizational goals.

Benefits

Be part of groundbreaking projects that are pushing the boundaries of the industry.
Experience a collaborative and inclusive work environment that highly appreciates your expertise.
Unlock your full potential with professional growth and development opportunities.
Enjoy work-life balance and flexible working hours.
Health, Vision & Dental Insurance.
Tuition Reimbursement.
Vacation/Holiday/Sick Time.
Flexible Spending & Health Savings Accounts.
401(k) with Company match.
Pet Insurance.