senior research associate

Syngene International Limited

<div>
 Date: 5 Sept 2025
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 Location:
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 <br/>
 Bangalore, KA, IN, 560099
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 Custom Field 1: Dedicated Centre
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 <strong>
  Job Description
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  <br/>
 </strong>
 Designation: Senior Research Associate (9-II)
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 Job Location: Bangalore
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 Department: DDS-SATT
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 <strong>
  About Syngene
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  <br/>
 </strong>
 Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene&rsquo; s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&amp;D productivity, speed up time to market and lower the cost of innovation.
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 <strong>
  Job Purpose (1-2 Lines)
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 Purification Scientist to work as a team member in purification team.
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 Key Responsibilities: (Maximum 5-8 Points)
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 <ul>
  <li>
   Proven ability to independently develop analytical methods for both reverse-phase (achiral) and polar organic (chiral) separations, with experience in scaling up methods to preparative scale.
  </li>
  <li>
   Hands-on experience with preparative HPLC systems, including MS-based Prep HPLC; familiarity with LC-MS and UPLC techniques is a strong advantage.
  </li>
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   Skilled in performing minor instrument troubleshooting, calibrations, and recovery analyses as required.
  </li>
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   Excellent written and verbal communication skills.
  </li>
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   Strong adherence to company health, safety, and compliance protocols.
  </li>
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   Flexibility to undertake additional responsibilities from the Line Manager in alignment with business needs.
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  </li>
 </ul>
 Educational Qualification: M.Sc. in Chemistry / analytical chemistry
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 <strong>
  Technical/functional Skills: (Maximum 4-6 Points)
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 </strong>
 <ul>
  <li>
   Preparative HPLC,
  </li>
  <li>
   MS based Prep HPLC, LC-MS, UPLC and SFC is an advantage.
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  </li>
 </ul>
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  Experience
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 <ul>
  <li>
   3 to 5 years of hands-on experience in reverse phase Prep.HPLC or relevant area.
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  Behavioral Skills
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   Must have very good communication skills
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  Equal Opportunity Employer
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 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
</div>


SENIOR RESEARCH ASSOCIATE

Ray-CRO

<p><b>Job Title: Senior Clinical Research Associate (CRA)</b><br/><b>Location:</b> Riyadh, KSA<br/><b>Job Type:</b> Full-time</p><p><b>Job Description</b></p><p>We are seeking a highly motivated <b>Senior CRA</b> to join our team on behalf of a leading multinational organization. The selected candidate will be responsible for overseeing and managing clinical trials from initiation to close-out, ensuring compliance with protocols, regulatory requirements, and SOPs.</p><p><b>Key Responsibilities:</b></p><ul><li>Oversee and coordinate clinical trial activities including investigator selection, patient recruitment analysis, and preparation of study-related documentation (protocols, CRFs, IBs, informed consents, agreements).</li><li>Prepare and manage regulatory submissions and follow-up to ensure timely approvals.</li><li>Organize and conduct investigator start-up meetings and site initiation visits.</li><li>Ensure proper drug accountability at assigned clinical sites.</li><li>Verify CRF data entries against source documentation.</li><li>Ensure timely reporting and follow-up of all adverse events in accordance with protocol and applicable guidelines.</li><li>Monitor trial activities in line with the protocol, monitoring plan, and SOPs.</li><li>Plan, order, and manage clinical trial materials (CTMs) from sponsors.</li><li>Maintain accurate and up-to-date Trial Master Files (TMFs) in compliance with local, legal, and ethical standards.</li><li>Track completed CRFs and ensure timely transfer to data management.</li><li>Maintain essential project files including EC approvals, CVs, IBs, protocols, consent forms, lab ranges, and correspondence.</li><li>Deliver study-specific training to site staff and ensure effective ongoing communication.</li><li>Escalate quality concerns to the Clinical Operations Manager (COM) and ensure corrective measures are implemented.</li><li>Document site management activities, monitoring visit findings, and follow-up actions through detailed reports.</li><li>Support patient recruitment strategies via investigator engagement, newsletters, and awareness initiatives.</li><li>Collaborate closely with the COM and assume delegated responsibilities when required.</li><li>Supervise and mentor CRAs and clinical trial assistants, providing guidance and training as needed.</li><li>Report any instances of GCP non-compliance, misconduct, or fraud appropriately.</li><li>Actively participate in departmental planning and contribute to continuous process improvement.</li></ul><p><b>Qualifications:</b></p><ul><li><b>Education:</b> Degree in Pharmacy or Medicine.</li><li><b>Experience:</b> Minimum of 2 years in clinical research.</li><li><b>Residency:</b> Based in Riyadh, KSA.</li></ul><p>Job Type: Full-time</p>

Senior clinical research Associate

AbbVie

<div><div><p>Senior Clinical Research Associate
</p></div><div><div><p>Montgomery, AL</p>
</div></div><div><div><ul><li><b>Function: </b>Research &amp; Development
</li></ul></div></div><div><div><ul><li><b>Job Type:</b> Full-time
</li></ul></div></div><p>Job ID: R00134142</p></div><p></p>
<br><div><p>Company Description</p><p><br>
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio.</p><p><br>
Job Description</p><p><br>
The Senior CRA will enable AbbVie&rsquo; s emergence as a world class R&amp;D organization, the position plays a key role in ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of studies.</p><p><b>
Responsibilities:</b></p><ul><li>
For assigned sites/study(s), ensure successful protocol level execution of SMM deliverables involving start-up, execution, and close-out.</li><li>
Ensure site related study execution including but not limited to monitoring visits, site evaluations, site selection, and activation, and monitoring close out and visit reports.</li><li>
Anticipate and identify site issues that could affect timelines and develop alternative solutions.</li><li>
Ensure clinical trial management systems containing all site-specific information are maintained and kept current. Provide Local regulatory and legal requirement expertise.</li><li>
Ensures timely payment execution for the assigned sites/study(s) according to the clinical study agreements and as per local requirements.</li><li>
Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Stay abreast of new and/or evolving local regulations, guidelines and policies.</li><li>
Ensure audit and inspection readiness of assigned sites.</li><li>
Advise on pre-audit activities for GCP requirements.</li><li>
Prepare and follow up site audits/inspections; provide input into the CAPA preparation.</li><li>
Responsible for coaching and mentoring CRAs and providing input into their development. Responsible for mentoring CRAs for various aspects of work.</li><li>
May be responsible for being the country point of contact for CROs for an assigned study.</li><li>
May participate/lead in global/local task forces and initiatives.</li><li>
Responsible for activities as assigned by manager.</li><li>
If assigned; Responsible for identifying training needs and standardizing and facilitating training solutions for SMM monitors globally.</li><li>
Provide consistent best practice approach to onboarding, consolidating &ldquo;lessons learned&rdquo; across areas and incorporating into monitoring training materials, defining best practice training curriculum, and maintaining awareness of upcoming changes to ensure effective training is delivered in a timely manner.</li><li>
If assigned; With guidance, may serve as key point of contact in country/district for assigned study. Update Impact/Tesla with country level information: Country-level planning timelines, LSR assignments, etc.</li><li>
If assigned; Global Representative for a single or multiple studies, collaborating with key stakeholders to achieve proactive, strategic and tactical success throughout the study planning, execution, and closeout phases leading to World Class clinical trials.</li><li>
If assigned; Responsible for remote data review of assigned sites/studies according to the Integrated Data Review Plan (IDRP), Monitoring Plan, SOP/WI and in accordance with the study timelines and objectives. Provides feedback on investigators/sites on an on-going basis based on the site performance. Interacts and builds professional and collaborative relationships with peers and site monitors</li></ul><p><br>
Qualifications</p><p><b><br>
Minimum Qualifications:</b></p><ul><li>
Bachelors degree</li><li>
3+ years of Site Monitoring Experience</li></ul><p><b>
Preferred Qualifications:</b></p><ul><li>
Health Related degree: e.g. Medical, Scientific, Nursing, Pharmacy</li></ul><p><b>
Other Required Skills:</b></p><ul><li>
Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and drive smart decision making.</li><li>
Excellent interpersonal skills with the ability to communicate persuasively and with clarity, flexibility and adaptability to changing requirements, resourcefulness and creativity.</li><li>
Demonstrated proactive and positive team player.</li><li>
Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with competing projects and deadlines.</li><li>
Demonstrated business ethics and integrity.</li></ul><p><br>
Additional Information</p><p><br>
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
</p><ul><li><p>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
</p></li><li><p>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
</p></li><li><p>This job is eligible to participate in our short-term incentive programs.
</p></li><li><p>This job is eligible to participate in our long-term incentive programs
</p></li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company&rsquo;s sole and absolute discretion, consistent with applicable law.</p><div></div><p>
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.</p><p>
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><p>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p>
https://www.abbvie.com/join-us/reasonable-accommodations.html</p></div>

SENIOR CLINICAL RESEARCH ASSOCIATE

BeOne Medicines

<div><div>BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.</div><div></div><ul><li><div>
The Sr. CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs.</div></li><li><div>
Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region.</div></li><li><div>
The Sr. CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained.</div></li><li><div>
Identify gaps and areas for improvement and propose CAPA.</div></li><li><div>
Supports start-up and provides local expertise.</div></li><li><div>
SSU experience is considered a plus</div></li></ul><div></div><div>
Activities:</div><ul><li><div>
Perform feasibility, site identification, selection and evaluation, supporting initial list of sites and recruitment targets</div></li><li><div>
Provides protocol and related study training to assigned sites.</div></li><li><div>
Conducts monitoring (pre-study, initiation, routine monitoring and closeout visits per monitoring plan and applicable SOPs</div></li><li><div>
Conducts co-monitoring visits, if required</div></li><li><div>
Completes monitoring visit reports in accordance with ICH-GCP, BeOne standards and SOP</div></li><li><div>
Manages sites and site performance by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.</div></li><li><div>
Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations</div></li><li><div>
Ensure inspection readiness of the study and sites</div></li><li><div>
Collaborates with Regional Clinical Operations Manager and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.)</div></li><li><div>
Attends disease indication project specific training and general CRA training as required</div></li><li><div>
Facilitate Study Oversight Visits (SOVs), site audits and/or inspections, as required</div></li><li><div>
Evaluates the quality and integrity of site practices &ndash; escalating quality and/or GCP issues with Investigators and internal team as appropriate.</div></li><li><div>
Anticipate and identify site issues; propose corrective and preventative actions; identify gaps and utilize opportunities. Constantly strive for operating excellence, question status-quo and promote innovation.</div></li></ul><div></div><div>
Education Required:</div><ul><li><div>
BS in a relevant scientific discipline and 2-5 years of monitoring experience.</div></li><li><div>
Experience in oncology global trials preferred</div></li></ul><div></div><div>
Computer Skills: Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook</div><div></div><div>
Other Qualifications:</div><div></div><ul><li><div>
Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines</div></li><li><div>
5+ years of (CRA) monitoring experience in the pharmaceutical or CRO industry</div></li><li><div>
Experience in oncology/hematology trials preferred</div></li><li><div>
Excellent communication and interpersonal skills</div></li><li><div>
Excellent organizational skills and ability to prioritize and multi-task</div></li><li><div>
Fluent in Turkish &amp; English (writing and speaking)</div></li></ul><div></div><div>
Travel: up to 60%</div><div></div><div>
Global Competencies</div><div>
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.</div><ul><li>
Fosters Teamwork</li><li>
Provides and Solicits Honest and Actionable Feedback</li><li>
Self-Awareness</li><li>
Acts Inclusively</li><li>
Demonstrates Initiative</li><li>
Entrepreneurial Mindset</li><li>
Continuous Learning</li><li>
Embraces Change</li><li>
Results-Oriented</li><li>
Analytical Thinking/Data Analysis</li><li>
Financial Excellence</li><li>
Communicates with Clarity</li></ul><div></div><div>
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.</div></div><div></div>

Senior Clinical Research Associate

Montefiore Einstein

<div><p><b>City/State:
</b></p>Bronx, New York
<p><b>Grant Funded:
</b></p>Yes
<p><b>Department:
</b></p>Cancer Clinical Trials Office
<p><b>Work Shift:
</b></p>Day
<p><b>Work Days:
</b></p>MON-FRI
<p><b>Scheduled Hours:
</b></p>9 AM-5:30 PM
<p><b>Scheduled Daily Hours:
</b></p>7.5 HOURS
<p><b>Pay Range:
</b></p>$68,000.00-$85,000.00
<p></p><p>The Cancer Clinical Trials <b>Senior Research Associate </b>supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate is able to function independently and is the lead Research Associate for the disease group which includes mentoring, training and reviewing/auditing accuracy of data of the junior Research Associates. The Senior Research Associate ensures timely collection of protocol data and samples including shipment to outside entities as required. This individual obtains informed consent of non-interventional studies, collects, maintains and organizes study information including compilation, registration and submission of data, as required by the Sponsor. Attends clinic as needed to perform activities including but not limited to assisting the research team with recruitment activities, administering questionnaires. Contributes to the development of research protocols and understanding research design including assists with database enhancements.<br>
</p><p></p><p><b>EDUCATION, TRAINING, LICENSES, REGISTRATIONS, PROFESSIONAL CERTIFICATIONS, AND WORK EXPERIENCE
</b></p><p>Bachelor Degree required - Bachelor's degree in life science or public health, preferred
</p><p>Masters Degree preferred
</p><p>Medical Degree (or foreign equivalent), Preferred
</p><p>ACRP (or SOCRA) certification required within 18 months of employment
</p><p>3 years of work experience required
</p><p>GCP training required
</p><p>MS Office proficient.
</p><p>Life Sciences or Public Health background preferred.
</p><p>Excellent written and oral communication skills
</p><p>Exceptional attention to detail and accuracy
</p><p>Ability to manage multiple tasks &amp; priorities
</p><p>Demonstrated leadership potential
</p><p>Knowledge of variety of concepts, practices and procedures in directly related field
</p><p></p>Montefiore Medical Center is an equal employment opportunity employer. Montefiore Medical Center will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law.</div>

Research Associate III

PwC India

<div>
 <p>
  <strong>
   Line of Service
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  Advisory
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   <strong>
    Industry/Sector
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   FS X-Sector
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    <strong>
     Specialism
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    </strong>
    Operations
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    <p>
     <strong>
      Management Level
      <br/>
     </strong>
     Senior Associate
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     <p>
      <strong>
       Job Description &amp; Summary
       <br/>
      </strong>
      A career within Application and Emerging Technology services, will provide you with a unique opportunity to help our clients identify and prioritise emerging technologies that can help solve their business problems. We help clients design approaches to integrate new technologies, skills, and processes so they can get the most out of their technology investment and drive business results and innovation.
      <br/>
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      <strong>
       Responsibilities
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      </strong>
      As a Senior Associate, you&rsquo;ll work as part of a team of problem solvers with extensive consulting and industry experience, helping our clients solve their complex business issues from strategy to execution. Specific responsibilities include but are not limited to:
      <br/>
      <ul>
       <li>
        Proactively assist in the management of several clients, while reporting to Managers and above
       </li>
       <li>
        Train and lead staff
       </li>
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        Establish effective working relationships directly with clients
       </li>
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        Contribute to the development of your own and team&rsquo;s technical acumen
       </li>
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        Keep up to date with local and national business and economic issues
       </li>
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        Be actively involved in business development activities to help identify and research opportunities on new/existing clients&nbsp;
       </li>
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        Continue to develop internal relationships and your PwC brand
        <br/>
       </li>
      </ul>
      <strong>
       Required Skills
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       Optional Skills
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         Desired Languages
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       <em>
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         (If blank, desired languages not specified)
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       <p>
        <strong>
         Travel Requirements
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        </strong>
        Up to 40%
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        <p>
         <strong>
          Available for Work Visa Sponsorship?
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         </strong>
         No
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         <p>
          <strong>
           Government Clearance Required?
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          </strong>
          No
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           <strong>
            Job Posting End Date
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      </p>
     </p>
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   </p>
  </p>
 </p>
</div>


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