Role Description
We are seeking a Study Start-Up Associate, level I or II dependent upon experience. This is a remote position. You will serve as the primary point of contact to study sites during start-up, work in a team setting managing multiple clinical study protocols and will be responsible for all regulatory tasks pertaining to assigned studies. This role will be involved in studies from start-up through maintenance and closeout.
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Reviews Sample and Site Informed Consent forms for compliance with the rules and regulations set forth by the FDA.
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Reviewing and approving site activation packages.
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Ensure that all assigned start-up activities are on track and support study deliverables.
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Maintaining accurate, complete and current information in the appropriate databases.
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Organizes regulatory information and tracks study documents.
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Collecting and reviewing regulatory documents for completeness and compliance to the rules and regulations set forth by the FDA and the study sponsor.
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Filing in eTMF system and accurate Trial Master File Maintenance.
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Maintains consistent site follow-up and ensures documents required are collected in a timely manner.
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Ensuring optimal efficiency to reduce start-up timelines and identify opportunities for continuous improvement.
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Researches regulatory issues and provides guidance and advice to colleagues.
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Participates in various start-up and Sponsor Kick-Off meetings.
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Escalate study issues appropriately and in a timely manner.
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Performs other duties as assigned.
Qualifications
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Bachelorβs degree required, preferably in a life science field or equivalent.
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1-4 years prior work experience required.
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Oncology clinical trials experience required.
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Randomized (larger trials) experience required.
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Prior experience in a CRO/pharmaceutical environment preferred.
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Prior Informed consent and Regulatory document review experience required.
Requirements
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Proficient knowledge of Word and Excel.
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Detail oriented.
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Knowledge of eTMF preferred.
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Excellent verbal and written communication skills.
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Fluent knowledge of written and verbal English.
Skills and Competencies needed
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Self-motivated, leverage resources to complete work efficiently, using time effectively.
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Takes a systematic approach to problem solving.
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Highly organized ability to prioritize tasks and track assignments to meet the needs of internal and external customers.
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Demonstrate openness and honesty while acting in accordance with moral, ethical, professional guidelines.
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The ability to convey or share ideas in concise terms that others understand.
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Correctly interprets messages, asks questions when clarification is needed.
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Is adaptable and flexible to changes with a positive attitude and a willingness to learn new ways to accomplish work activities and objectives.
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Ability to adjust and reprioritize with the needs of Theradex Oncology.
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Works with others to establish and maintain a positive working relationship while offering added value and insight.
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Working collaboratively with others to agree on outcomes and actions to complete tasks or achieve goals.
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Demonstrated persistence in bringing issues to closure.
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Views situations from multiple perspectives and potential impact outside oneβs area.
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Uses appropriate interpersonal style to gain acceptance of ideas and plans.
Benefits
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Comprehensive benefits package including medical, dental and vision coverage.
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Life insurance and disability insurance (STD/LTD).
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Company matched 401(k).
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Very competitive tuition reimbursement.
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Generous vacation/sick plans.
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Flexible work schedules.
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Employee discounts and other company provided benefits.
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Annual base salary ranges from $60,000-$105,000 with bonus potential.