Clinical Contract Associate

EntryOncology
$60K - $80K/yr(estimated)

Description

<span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.</span></span><br>&#160;<p><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">For assigned studies, the Contract Associate is responsible for completing site contract and budget negotiations with sites participating in SystImmune clinical trials. This is included but not limited to Sites&#8217; proposed changes to standard contract terms and the study-specific budget parameters (in partnership with other business lines internally), (3) ensuring the delivery of high quality, compliant, effective, and timely site contracts, and (4) maintaining productive relationships with internal stakeholders and sites.</span></span></p><p><br><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;"><strong>Key Responsibilities</strong></span></span></p><ul><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">&#160;Accountable for negotiating clinical contracts within timelines with sites and Principal Investigators and site study staff</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Address changes to study scope to ensure timely contract amendments during the duration of Clinical Trials</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Negotiate Site facing budgets within approved parameters</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">As a member of cross-functional study team, present on agenda topics related to contract and budget status of the SSU meetings as related to clinical contracting</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Single point of contact for internal stakeholders, and CROs, when applicable, and sites for assigned studies in North America</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Accountable for ensuring that performance and efficiency standards are met for assigned studies</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Assist with filing SystImmune&#8217;s site contracts in the company repository as instructed</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Engage with the study teams from SSU and feasibility processes throughout the end-to-end contracting lifecycle</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Work closely with internal stakeholders, and CROs and effectively communicate, in order to ensure that business objectives are met (e.g., scheduled site initiation visit deadlines)</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Handle site contracting related escalations from the CROs and/or the investigator sites, effectively and efficiently</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Develop and enhance relationships with internal stakeholders, CROs, and sites</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Ensure that internal systems are updated in a timely, accurate, and complete manner</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Meet with study teams regularly and prioritize assignments</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Execute changes related to study protocol amendments, ensuring timely contract amendment and implementation</span></span></li></ul><br><strong><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Qualifications</span></span></strong><ul><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Required minimum of 2 years of relevant experience with clinical site contracting at a biopharmaceutical company, Clinical Research Site or CRO</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Strong negotiation skills</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Strong verbal and written communication in English</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Ability to work in a fast-paced working environment</span></span></li><li><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">Bachelor&#8217;s Degree in scientific discipline, law, finance or related field</span></span></li></ul><p></p><p><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;">This job description has been designed to capture the essential functions of this job. It was not designed to contain or be interpreted as a comprehensive inventory of all the duties, responsibilities and qualifications required to perform this job. It is based on management&#8217;s assessment of the requirements and functions of the job as of the date this description was prepared.</span></span><br><br><strong>Compensation and Benefits:</strong><br>The expected base salary range for this position is <strong>$60,000 - $80,000</strong> annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate&#8217;s qualifications, experience, and skills.<br><br>While most offers typically fall within the&#160;low to mid-point&#160;of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.<br>&#160;<br><strong>SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company&#8217;s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.<br>&#160;<br>We offer an opportunity for you to learn and grow while making significant contributions to the company&#8217;s success.<br>&#160;<br>SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.</strong><br>&#160;</p>
SystImmune

SystImmune

BIOTECHNOLOGY

Novel therapeutic bi-specific, and multi-specific antibodies, antibody-drug conjugates

LocationWA - Redmond
Open Jobs46
OncologyNeurology
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